1: SLC23A1  
Official Symbol SLC23A1 and Name: solute carrier family 23 (nucleobase transporters), member 1 [Homo sapiens]
Other Aliases: MGC22361, SLC23A2, SVCT1, YSPL3
Other Designations: Na(+)/L-ascorbic acid transporter 1; sodium-dependent vitamin C transporter-1; solute carrier family 23 (nucleobase transporters), member 2; yolk sac permease-like molecule 3
Chromosome: 5; Location: 5q31.2-q31.3
Annotation: Chromosome 5, NC_000005.8 (138730787..138746900, complement)
MIM: 603790
GeneID: 9963
2: SLC23A2  
Official Symbol SLC23A2 and Name: solute carrier family 23 (nucleobase transporters), member 2 [Homo sapiens]
Other Aliases: RP1-237C24.1, KIAA0238, NBTL1, SLC23A1, SVCT2, YSPL2
Other Designations: Na(+)/L-ascorbic acid transporter 2; sodium-dependent vitamin C transporter-2; solute carrier family 23 (nucleobase transporters), member 1; yolk sac permease-like molecule 2
Chromosome: 20; Location: 20p13
Annotation: Chromosome 20, NC_000020.9 (4781002..4938939, complement)
MIM: 603791
GeneID: 9962
3: SLC3A1  
Official Symbol SLC3A1 and Name: solute carrier family 3 (cystine, dibasic and neutral amino acid transporters, activator of cystine, dibasic and neutral amino acid transport), member 1 [Homo sapiens]
Other Aliases: ATR1, CSNU1, D2H, FLJ34681, NBAT, RBAT
Other Designations: SLC3A1 variant B; SLC3A1 variant C; SLC3A1 variant D; SLC3A1 variant E; SLC3A1 variant F; SLC3A1 variant G; amino acid transporter 1; solute carrier family 3 (cystine, dibasic and neutral amino acid transporters), member 1; solute carrier family 3, member 1
Chromosome: 2; Location: 2p16.3
Annotation: Chromosome 2, NC_000002.10 (44356103..44401448)
MIM: 104614
GeneID: 6519
4: SLC12A8  
Official Symbol SLC12A8 and Name: solute carrier family 12 (potassium/chloride transporters), member 8 [Homo sapiens]
Other Aliases: CCC9, DKFZp686L18248, FLJ23188
Other Designations: cation-chloride cotransporter 9; solute carrier family 12 (sodium/potassium/chloride transporters), member 8; solute carrier family 12, member 8
Chromosome: 3
Annotation: Chromosome 3, NC_000003.10 (126284172..126414273, complement)
GeneID: 84561
5: SLC16A2
Official Symbol SLC16A2 and Name: solute carrier family 16, member 2 (monocarboxylic acid transporter 8) [Homo sapiens]
Other Aliases: RP11-449M9.1, AHDS, DXS128, DXS128E, MCT7, MCT8, XPCT
Other Designations: Allan-Herndon-Dudley syndrome; X-linked PEST-containing transporter; monocarboxylate transporter 8; solute carrier family 16 (monocarboxylic acid transporters), member 2; solute carrier family 16 (monocarboxylic acid transporters), member 2 (putative transporter); solute carrier family 16, member 2
Chromosome: X; Location: Xq13.2
Annotation: Chromosome X, NC_000023.9 (73557810..73670475)
MIM: 300095
GeneID: 6567
6: SLC29A1  
Official Symbol SLC29A1 and Name: solute carrier family 29 (nucleoside transporters), member 1 [Homo sapiens]
Other Aliases: ENT1, MGC1465, MGC3778
Other Designations: equilibrative nitrobenzylmercaptopurine riboside (NBMPR)-sensitive nucleoside transporter; equilibrative nucleoside transporter 1; nucleoside transporter, es-type; solute carrier family 29, member 1
Chromosome: 6; Location: 6p21.2-p21.1
Annotation: Chromosome 6, NC_000006.10 (44295371..44309856)
MIM: 602193
GeneID: 2030
7: SLC29A4  
Official Symbol SLC29A4 and Name: solute carrier family 29 (nucleoside transporters), member 4 [Homo sapiens]
Other Aliases: ENT4, FLJ34923, PMAT
Other Designations: equilibrative nucleoside transporter 4; plasma membrane monoamine transporter
Chromosome: 7; Location: 7p22.1
Annotation: Chromosome 7, NC_000007.12 (5289101..5310216)
MIM: 609149
GeneID: 222962
8: SLC29A2  
Official Symbol SLC29A2 and Name: solute carrier family 29 (nucleoside transporters), member 2 [Homo sapiens]
Other Aliases: DER12, ENT2, HNP36
Other Designations: equilibrative nucleoside transporter 2; hydrophobic nucleolar protein, 36kD
Chromosome: 11; Location: 11q13
Annotation: Chromosome 11, NC_000011.8 (65886568..65895867, complement)
MIM: 602110
GeneID: 3177
9: SLC29A3  
Official Symbol SLC29A3 and Name: solute carrier family 29 (nucleoside transporters), member 3 [Homo sapiens]
Other Aliases: ENT3, FLJ11160
Other Designations: equilibrative nucleoside transporter 3
Chromosome: 10; Location: 10q22.1
Annotation: Chromosome 10, NC_000010.9 (72749038..72793148)
GeneID: 55315
10: SLC31A1  
Official Symbol SLC31A1 and Name: solute carrier family 31 (copper transporters), member 1 [Homo sapiens]
Other Aliases: COPT1, CTR1, MGC75487, hCTR1
Other Designations: copper transport 1 homolog; copper transporter 1
Chromosome: 9; Location: 9q31-q32
Annotation: Chromosome 9, NC_000009.10 (115023689..115066593)
MIM: 603085
GeneID: 1317
11: SLC12A9  
Official Symbol SLC12A9 and Name: solute carrier family 12 (potassium/chloride transporters), member 9 [Homo sapiens]
Other Aliases: CIP1, FLJ46905
Other Designations: cation-chloride cotransporter-interacting protein; cation-chloride cotransporter-interacting protein 1
Chromosome: 7; Location: 7q22
Annotation: Chromosome 7, NC_000007.12 (100288294..100302569)
GeneID: 56996
12: SLC12A4  
Official Symbol SLC12A4 and Name: solute carrier family 12 (potassium/chloride transporters), member 4 [Homo sapiens]
Other Aliases: FLJ40489, KCC1
Other Designations: potassium transport protein; potassium/chloride cotransporter 1
Chromosome: 16; Location: 16q22.1
Annotation: Chromosome 16, NC_000016.8 (66535731..66560026, complement)
MIM: 604119
GeneID: 6560
13: SLC12A3  
Official Symbol SLC12A3 and Name: solute carrier family 12 (sodium/chloride transporters), member 3 [Homo sapiens]
Other Aliases: NCCT, TSC
Other Designations: thiazide-sensitive Na-Cl cotransporter
Chromosome: 16; Location: 16q13
Annotation: Chromosome 16, NC_000016.8 (55456643..55504850)
MIM: 600968
GeneID: 6559
14: SLC12A2  
Official Symbol SLC12A2 and Name: solute carrier family 12 (sodium/potassium/chloride transporters), member 2 [Homo sapiens]
Other Aliases: BSC, BSC2, MGC104233, NKCC1
Other Designations: basolateral Na-K-Cl symporter; bumetanide-sensitive sodium-(potassium)-chloride cotransporter 1
Chromosome: 5; Location: 5q23.3
Annotation: Chromosome 5, NC_000005.8 (127447382..127553279)
MIM: 600840
GeneID: 6558
15: SLC5A3  
Official Symbol SLC5A3 and Name: solute carrier family 5 (inositol transporters), member 3 [Homo sapiens]
Other Aliases: SMIT, SMIT2
Other Designations: human solute carrier family 5, member 3, Sodium/myo-inositol cotransporter; sodium/myo-inositol cotransporter 1; solute carrier family 5 (inositol transporter), member 3
Chromosome: 21; Location: 21q22.12
Annotation: Chromosome 21, NC_000021.7 (34389368..34391524)
MIM: 600444
GeneID: 6526
16: SLC31A2  
Official Symbol SLC31A2 and Name: solute carrier family 31 (copper transporters), member 2 [Homo sapiens]
Other Aliases: COPT2, CTR2, hCTR2
Other Designations: copper transporter 2
Chromosome: 9; Location: 9q31-q32
Annotation: Chromosome 9, NC_000009.10 (114953122..114966225)
MIM: 603088
GeneID: 1318
17: SLC12A7  
Official Symbol SLC12A7 and Name: solute carrier family 12 (potassium/chloride transporters), member 7 [Homo sapiens]
Other Aliases: DKFZP434F076, KCC4
Other Designations: potassium/chloride transporter KCC4
Chromosome: 5; Location: 5p15
Annotation: Chromosome 5, NC_000005.8 (1103499..1165109, complement)
MIM: 604879
GeneID: 10723
18: SLC23A3  
Official Symbol SLC23A3 and Name: solute carrier family 23 (nucleobase transporters), member 3 [Homo sapiens]
Other Aliases: E2BP3, FLJ31168, SVCT3, Yspl1
Other Designations: E2-binding protein 3
Chromosome: 2; Location: 2q35
Annotation: Chromosome 2, NC_000002.10 (219734431..219742959, complement)
GeneID: 151295
19: SLC11A2  
Official Symbol SLC11A2 and Name: solute carrier family 11 (proton-coupled divalent metal ion transporters), member 2 [Homo sapiens]
Other Aliases: DCT1, DMT1, FLJ37416, NRAMP2
Other Designations: natural resistance-associated macrophage protein 2
Chromosome: 12; Location: 12q13
Annotation: Chromosome 12, NC_000012.10 (49666044..49706409, complement)
MIM: 600523
GeneID: 4891
20: SLC12A1  
Official Symbol SLC12A1 and Name: solute carrier family 12 (sodium/potassium/chloride transporters), member 1 [Homo sapiens]
Other Aliases: BSC1, MGC48843, NKCC2
Other Designations: Na-K-2Cl cotransporter; sodium potassium chloride cotransporter 2
Chromosome: 15; Location: 15q15-q21.1
Annotation: Chromosome 15, NC_000015.8 (46287190..46382417)
MIM: 600839
GeneID: 6557
21: SLC11A1  
Official Symbol SLC11A1 and Name: solute carrier family 11 (proton-coupled divalent metal ion transporters), member 1 [Homo sapiens]
Other Aliases: LSH, NRAMP, NRAMP1
Other Designations: natural resistance-associated macrophage protein 1; solute carrier family 11 (sodium/phosphate symporters), member 1
Chromosome: 2; Location: 2q35
Annotation: Chromosome 2, NC_000002.10 (218955161..218968741)
MIM: 600266
GeneID: 6556
22: SLC16A10  
Official Symbol SLC16A10 and Name: solute carrier family 16, member 10 (aromatic amino acid transporter) [Homo sapiens]
Other Aliases: PRO0813, TAT1
Other Designations: T-type amino acid transporter 1; solute carrier family 16 (monocarboxylic acid transporters), member 10; solute carrier family 16, member 10
Chromosome: 6; Location: 6q21-q22
Annotation: Chromosome 6, NC_000006.10 (111515502..111650907)
MIM: 607550
GeneID: 117247
23: SLC31A1P
Official Symbol SLC31A1P and Name: solute carrier family 31 (copper transporters), member 1 pseudogene [Homo sapiens]
Other Aliases: CTR1P, CTR1psi
Chromosome: 3; Location: 3q25-q26
GeneID: 117151
24: LOC402509
similar to solute carrier family 29 (nucleoside transporters), member 4 [Homo sapiens]
Chromosome: 7; Location: 7p11.2
Annotation: Chromosome 7, NC_000007.12 (57084814..57092481, complement)
GeneID: 402509
25: LOC652058
similar to solute carrier family 29 (nucleoside transporters), member 4 [Homo sapiens]
Chromosome: Un
GeneID: 652058
26: LOC402269
similar to solute carrier family 29 (nucleoside transporters), member 4 [Homo sapiens]
Chromosome: 7; Location: 7q11.21
Annotation: Chromosome 7, NC_000007.12 (62730421..62783364)
GeneID: 402269
27: LOC728500
similar to solute carrier family 29 (nucleoside transporters), member 4 [Homo sapiens]
Chromosome: 7; Location: 7p11.2
Annotation: Chromosome 7, NC_000007.12 (57009071..57016002, complement)
GeneID: 728500
28: SLC16A12
Official Symbol SLC16A12 and Name: solute carrier family 16, member 12 (monocarboxylic acid transporter 12) [Homo sapiens]
Other Aliases: RP11-168O10.10, DKFZp686E188, MCT12
Other Designations: solute carrier family 16 (monocarboxylic acid transporters), member 12
Chromosome: 10; Location: 10q23.31
Annotation: Chromosome 10, NC_000010.9 (91180753..91285293, complement)
GeneID: 387700
29: LOC654078
similar to solute carrier family 29 (nucleoside transporters), member 4 [Homo sapiens]
Chromosome: 7
GeneID: 654078
30: LOC346887
similar to solute carrier family 16 (monocarboxylic acid transporters), member 14 [Homo sapiens]
Chromosome: 8; Location: 8q23.1
Annotation: Chromosome 8, NC_000008.9 (107347604..107354297)
GeneID: 346887
31: SLC23A4
Official Symbol SLC23A4 and Name: solute carrier family 23 (nucleobase transporters), member 4 [Homo sapiens]
Chromosome: 7; Location: 7q33
Annotation: Chromosome 7, NC_000007.12 (134612510..134648854, complement)
GeneID: 641842
32: SLC12A6  
Official Symbol SLC12A6 and Name: solute carrier family 12 (potassium/chloride transporters), member 6 [Homo sapiens]
Other Aliases: ACCPN, DKFZP434D2135, KCC3, KCC3A, KCC3B
Other Designations: agenesis of corpus callosum and peripheral neuropathy (Andermann syndrome); potassium chloride cotransporter 3; potassium chloride cotransporter KCC3a-S3; solute carrier family 12, member 6
Chromosome: 15; Location: 15q13-q15
Annotation: Chromosome 15, NC_000015.8 (32312958..32398222, complement)
MIM: 604878
GeneID: 9990
33: SLC16A14  
Official Symbol SLC16A14 and Name: solute carrier family 16, member 14 (monocarboxylic acid transporter 14) [Homo sapiens]
Other Aliases: FLJ30794, MCT14
Other Designations: monocarboxylate transporter 14; solute carrier family 16 (monocarboxylic acid transporters), member 14
Chromosome: 2; Location: 2q36.3
Annotation: Chromosome 2, NC_000002.10 (230607942..230641863, complement)
GeneID: 151473
34: SLC16A9  
Official Symbol SLC16A9 and Name: solute carrier family 16, member 9 (monocarboxylic acid transporter 9) [Homo sapiens]
Other Aliases: C10orf36, FLJ43803, MCT9
Other Designations: monocarboxylate transporter 9; solute carrier family 16 (monocarboxylic acid transporters), member 9
Chromosome: 10; Location: 10q21.1
Annotation: Chromosome 10, NC_000010.9 (61080529..61165766, complement)
GeneID: 220963
35: SLC16A13  
Official Symbol SLC16A13 and Name: solute carrier family 16, member 13 (monocarboxylic acid transporter 13) [Homo sapiens]
Other Aliases: MCT13
Other Designations: monocarboxylate transporter 13; solute carrier family 16 (monocarboxylic acid transporters), member 13
Chromosome: 17; Location: 17p13.1
Annotation: Chromosome 17, NC_000017.9 (6880426..6884005)
GeneID: 201232
36: SLC16A8
Official Symbol SLC16A8 and Name: solute carrier family 16, member 8 (monocarboxylic acid transporter 3) [Homo sapiens]
Other Aliases: MCT3, REMP
Other Designations: OTTHUMP00000028510; monocarboxylate transporter 3; solute carrier 16 (monocarboxylic acid transporters), member 8; solute carrier family 16, member 8
Chromosome: 22; Location: 22q12.3-q13.2
Annotation: Chromosome 22, NC_000022.9 (36804090..36809095, complement)
MIM: 610409
GeneID: 23539
37: SLC16A7  
Official Symbol SLC16A7 and Name: solute carrier family 16, member 7 (monocarboxylic acid transporter 2) [Homo sapiens]
Other Aliases: MCT2
Other Designations: monocarboxylate transporter 2; solute carrier family 16 (monocarboxylic acid transporters), member 7; solute carrier family 16, member 7
Chromosome: 12; Location: 12q13
Annotation: Chromosome 12, NC_000012.10 (58369393..58461675)
MIM: 603654
GeneID: 9194
38: SLC16A3  
Official Symbol SLC16A3 and Name: solute carrier family 16, member 3 (monocarboxylic acid transporter 4) [Homo sapiens]
Other Aliases: MCT3, MCT4, MGC138472, MGC138474
Other Designations: monocarboxylate transporter 3; monocarboxylate transporter 4; solute carrier family 16 (monocarboxylic acid transporters), member 3; solute carrier family 16, member 3
Chromosome: 17; Location: 17q25
Annotation: Chromosome 17, NC_000017.9 (77780236..77794777)
MIM: 603877
GeneID: 9123
39: SLC16A4  
Official Symbol SLC16A4 and Name: solute carrier family 16, member 4 (monocarboxylic acid transporter 5) [Homo sapiens]
Other Aliases: MCT4, MCT5
Other Designations: monocarboxylate transporter 4; monocarboxylate transporter 5; solute carrier family 16 (monocarboxylic acid transporters), member 4; solute carrier family 16, member 4
Chromosome: 1; Location: 1p13.3
Annotation: Chromosome 1, NC_000001.9 (110707028..110735159, complement)
MIM: 603878
GeneID: 9122
40: SLC16A5  
Official Symbol SLC16A5 and Name: solute carrier family 16, member 5 (monocarboxylic acid transporter 6) [Homo sapiens]
Other Aliases: MCT5, MCT6
Other Designations: monocarboxylate transporter 5; monocarboxylate transporter 6; solute carrier family 16 (monocarboxylic acid transporters), member 5; solute carrier family 16, member 5
Chromosome: 17; Location: 17q25.1
Annotation: Chromosome 17, NC_000017.9 (70595650..70613847)
MIM: 603879
GeneID: 9121
41: SLC16A6  
Official Symbol SLC16A6 and Name: solute carrier family 16, member 6 (monocarboxylic acid transporter 7) [Homo sapiens]
Other Aliases: MCT6, MCT7
Other Designations: monocarboxylate transporter 6; monocarboxylate transporter 7; solute carrier family 16 (monocarboxylic acid transporters), member 6; solute carrier family 16, member 6
Chromosome: 17; Location: 17q24.2
Annotation: Chromosome 17, NC_000017.9 (63775933..63799002, complement)
MIM: 603880
GeneID: 9120
42: SLC16A11  
Official Symbol SLC16A11 and Name: solute carrier family 16, member 11 (monocarboxylic acid transporter 11) [Homo sapiens]
Other Aliases: FLJ90193, MCT11
Other Designations: solute carrier family 16 (monocarboxylic acid transporters), member 11; solute carrier family 16, member 11
Chromosome: 17; Location: 17p13.1
Annotation: Chromosome 17, NC_000017.9 (6885673..6887966, complement)
GeneID: 162515
43: SLC16A1  
Official Symbol SLC16A1 and Name: solute carrier family 16, member 1 (monocarboxylic acid transporter 1) [Homo sapiens]
Other Aliases: FLJ36745, MCT, MCT1, MGC44475
Other Designations: monocarboxylate transporter 1; solute carrier family 16 (monocarboxylic acid transporters), member 1; solute carrier family 16, member 1
Chromosome: 1; Location: 1p12
Annotation: Chromosome 1, NC_000001.9 (113256377..113300328, complement)
MIM: 600682
GeneID: 6566
44: SLC5A4  
Official Symbol SLC5A4 and Name: solute carrier family 5 (low affinity glucose cotransporter), member 4 [Homo sapiens]
Other Aliases: DJ90G24.4, SAAT1, SGLT3
Other Designations: low affinity sodium glucose cotransporter; solute carrier family 5 (neutral amino acid transporters, system A), member 4
Chromosome: 22; Location: 22q12.2-q12.3
Annotation: Chromosome 22, NC_000022.9 (30944463..30981318, complement)
GeneID: 6527
45: SLC40A1  
Official Symbol SLC40A1 and Name: solute carrier family 40 (iron-regulated transporter), member 1 [Homo sapiens]
Other Aliases: FPN1, HFE4, IREG1, MST079, MSTP079, MTP1, SLC11A3
Other Designations: ferroportin 1; iron regulated gene 1; putative ferroportin 1 variant IIIB; solute carrier family 11 (proton-coupled divalent metal ion transporters), member 3
Chromosome: 2; Location: 2q32
Annotation: Chromosome 2, NC_000002.10 (190133561..190153858, complement)
MIM: 604653
GeneID: 30061
46: ABCC1
Official Symbol ABCC1 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 1 [Homo sapiens]
Other Aliases: ABC29, ABCC, DKFZp686N04233, DKFZp781G125, GS-X, MRP, MRP1
Other Designations: ATP-binding cassette, sub-family C, member 1; LTC4 transporter; leukotriene C(4) transporter; multidrug resistance protein; multiple drug resistance protein 1; multiple drug resistance-associated protein
Chromosome: 16; Location: 16p13.1
Annotation: Chromosome 16, NC_000016.8 (15950935..16143774)
MIM: 158343
GeneID: 4363
47: ABCG1  
Official Symbol ABCG1 and Name: ATP-binding cassette, sub-family G (WHITE), member 1 [Homo sapiens]
Other Aliases: ABC8, MGC34313, WHITE1
Other Designations: ABC transporter; ABC transporter 8; ATP-binding cassette sub-family G member 1; ATP-binding cassette transporter 8; ATP-binding cassette transporter member 1 of subfamily G; homolog of Drosophila white; white protein homolog; white protein homolog (ATP-binding cassette transporter 8)
Chromosome: 21; Location: 21q22.3
Annotation: Chromosome 21, NC_000021.7 (42492868..42590423)
MIM: 603076
GeneID: 9619
48: ABCA2
Official Symbol ABCA2 and Name: ATP-binding cassette, sub-family A (ABC1), member 2 [Homo sapiens]
Other Aliases: ABC2, MGC129761
Other Designations: ATP-binding cassette, sub-family A, member 2; OTTHUMP00000064733
Chromosome: 9; Location: 9q34
Annotation: Chromosome 9, NC_000009.10 (139021507..139043195, complement)
MIM: 600047
GeneID: 20
49: SLC41A3  
Official Symbol SLC41A3 and Name: solute carrier family 41, member 3 [Homo sapiens]
Other Aliases: FLJ20473, SLC41A1-L2
Other Designations: SLC41A1-like 2
Chromosome: 3; Location: 3q21.2
Annotation: Chromosome 3, NC_000003.10 (127207890..127285824, complement)
MIM: 610803
GeneID: 54946
50: ABCB4  
Official Symbol ABCB4 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 4 [Homo sapiens]
Other Aliases: ABC21, GBD1, MDR2, MDR2/3, MDR3, PFIC-3, PGY3
Other Designations: ATP-binding cassette, subfamily B, member 4; P glycoprotein 3/multiple drug resistance 3; P-glycoprotein-3/multiple drug resistance-3; multidrug resistance protein 3; multiple drug resistance 3
Chromosome: 7; Location: 7q21.1
Annotation: Chromosome 7, NC_000007.12 (86869297..86947684, complement)
MIM: 171060
GeneID: 5244
51: ABCD4  
Official Symbol ABCD4 and Name: ATP-binding cassette, sub-family D (ALD), member 4 [Homo sapiens]
Other Aliases: ABC41, EST352188, P70R, P79R, PMP69, PXMP1L
Other Designations: ATP-binding cassette, sub-family D, member 4; peroxisomal membrane protein 1-like
Chromosome: 14; Location: 14q24.3
Annotation: Chromosome 14, NC_000014.7 (73821881..73839420, complement)
MIM: 603214
GeneID: 5826
52: ABCC9
Official Symbol ABCC9 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 9 [Homo sapiens]
Other Aliases: ABC37, CMD1O, FLJ36852, SUR2
Other Designations: ATP-binding cassette, sub-family C, member 9; sulfonylurea receptor 2A
Chromosome: 12; Location: 12p12.1
Annotation: Chromosome 12, NC_000012.10 (21845245..21980875, complement)
MIM: 601439
GeneID: 10060
53: SLC26A1
Official Symbol SLC26A1 and Name: solute carrier family 26 (sulfate transporter), member 1 [Homo sapiens]
Other Aliases: EDM4, SAT-1, SAT1
Other Designations: solute carrier family 26, member 1; sulfate anion tranporter AT1; sulfate transporter; sulfate/anion transporter SAT-1 protein
Chromosome: 4; Location: 4p16.3
Annotation: Chromosome 4, NC_000004.10 (962861..977224, complement)
MIM: 610130
GeneID: 10861
54: ABCD2  
Official Symbol ABCD2 and Name: ATP-binding cassette, sub-family D (ALD), member 2 [Homo sapiens]
Other Aliases: ABC39, ALDL1, ALDR, ALDRP, hALDR
Other Designations: ATP-binding cassette, sub-family D, member 2; adrenoleukodystrophy-like 1
Chromosome: 12; Location: 12q11-q12
Annotation: Chromosome 12, NC_000012.10 (38232813..38300237, complement)
MIM: 601081
GeneID: 225
55: ABCG5
Official Symbol ABCG5 and Name: ATP-binding cassette, sub-family G (WHITE), member 5 (sterolin 1) [Homo sapiens]
Other Aliases: STSL
Other Designations: ATP-binding cassette, subfamily G, member 5; sterolin 1
Chromosome: 2; Location: 2p21
Annotation: Chromosome 2, NC_000002.10 (43893115..43919462, complement)
MIM: 605459
GeneID: 64240
56: ABCA7
Official Symbol ABCA7 and Name: ATP-binding cassette, sub-family A (ABC1), member 7 [Homo sapiens]
Other Aliases: ABCA-SSN, ABCX, FLJ40025
Other Designations: ATP-binding cassette, sub-family A, member 7; autoantigen SS-N; macrophage ABC transporter
Chromosome: 19; Location: 19p13.3
Annotation: Chromosome 19, NC_000019.8 (992245..1016571)
MIM: 605414
GeneID: 10347
57: ABCA4
Official Symbol ABCA4 and Name: ATP-binding cassette, sub-family A (ABC1), member 4 [Homo sapiens]
Other Aliases: ABC10, ABCR, ARMD2, CORD3, DKFZp781N1972, FFM, RMP, RP19, STGD, STGD1
Other Designations: ATP binding cassette transporter; ATP-binding cassette, sub-family A member 4; ATP-binding transporter, retina-specific; retina-specific ABC transporter; rim protein
Chromosome: 1; Location: 1p22.1-p21
Annotation: Chromosome 1, NC_000001.9 (94230981..94359267, complement)
MIM: 601691
GeneID: 24
58: ABCG2  
Official Symbol ABCG2 and Name: ATP-binding cassette, sub-family G (WHITE), member 2 [Homo sapiens]
Other Aliases: ABC15, ABCP, BCRP, BCRP1, BMDP, CDw338, EST157481, MGC102821, MRX, MXR, MXR1
Other Designations: ABC transporter; ATP-binding cassette sub-family G (WHITE) member 2; ATP-binding cassette transporter G2; ATP-binding cassette, sub-family G, member 2; breast cancer resistance protein; mitoxantrone resistance protein; placenta specific MDR protein
Chromosome: 4; Location: 4q22
Annotation: Chromosome 4, NC_000004.10 (89230440..89299035, complement)
MIM: 603756
GeneID: 9429
59: SLC45A4
Official Symbol SLC45A4 and Name: solute carrier family 45, member 4 [Homo sapiens]
Other Aliases: KIAA1126
Chromosome: 8; Location: 8q24.3
Annotation: Chromosome 8, NC_000008.9 (142286450..142333336, complement)
GeneID: 57210
60: ABCD3  
Official Symbol ABCD3 and Name: ATP-binding cassette, sub-family D (ALD), member 3 [Homo sapiens]
Other Aliases: ABC43, PMP70, PXMP1
Other Designations: ATP-binding cassette, sub-family D, member 3; Peroxisomal membrane protein-1 (70kD); dJ824O18.1 (ATP-binding cassette, sub-family D (ALD), member 3 (PMP70, PXMP1)); peroxisomal membrane protein 1 (70kD, Zellweger syndrome); peroxisomal membrane protein-1
Chromosome: 1; Location: 1p22-p21
Annotation: Chromosome 1, NC_000001.9 (94656599..94756672)
MIM: 170995
GeneID: 5825
61: ABCD1  
Official Symbol ABCD1 and Name: ATP-binding cassette, sub-family D (ALD), member 1 [Homo sapiens]
Other Aliases: ABC42, ALD, ALDP, AMN
Other Designations: adrenoleukodystrophy; adrenoleukodystrophy protein
Chromosome: X; Location: Xq28
Annotation: Chromosome X, NC_000023.9 (152643530..152663375)
MIM: 300371
GeneID: 215
62: ABCF1  
Official Symbol ABCF1 and Name: ATP-binding cassette, sub-family F (GCN20), member 1 [Homo sapiens]
Other Aliases: ABC27, ABC50
Other Designations: ATP-binding cassette 50; ATP-binding cassette 50 (TNF-alpha stimulated); ATP-binding cassette, sub-family F, member 1; TNFalpha-inducible ATP-binding protein
Chromosome: 6; Location: 6p21.33
Annotation: Chromosome 6, NC_000006.10 (30647149..30667288)
MIM: 603429
GeneID: 23
63: ABCA3
Official Symbol ABCA3 and Name: ATP-binding cassette, sub-family A (ABC1), member 3 [Homo sapiens]
Other Aliases: ABC-C, ABC3, EST111653, LBM180, MGC72201, SMDP3
Other Designations: ABC transporter 3; ATP-binding cassette 3; ATP-binding cassette, sub-family A member 3
Chromosome: 16; Location: 16p13.3
Annotation: Chromosome 16, NC_000016.8 (2265883..2330595, complement)
MIM: 601615
GeneID: 21
64: TAP2
Official Symbol TAP2 and Name: transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) [Homo sapiens]
Other Aliases: DAQB-69D7.2, ABC18, ABCB3, APT2, D6S217E, PSF2, RING11
Other Designations: ABC transporter, MHC 2; ATP-binding cassette, sub-family B (MDR/TAP), member 3; OTTHUMP00000038912; OTTHUMP00000038914; antigen peptide transporter 2; peptide supply factor 2; peptide transporter PSF2; transporter 2, ABC (ATP binding cassette); transporter 2, ATP-binding cassette, sub-family B
Chromosome: 6; Location: 6p21.3
Annotation: Chromosome 6, NC_000006.10 (32897588..32914525, complement)
MIM: 170261
GeneID: 6891
65: ABCC4  
Official Symbol ABCC4 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 4 [Homo sapiens]
Other Aliases: RP11-74A12.1, EST170205, MOAT-B, MOATB, MRP4
Other Designations: ATP-binding cassette, sub-family C, member 4; bA464I2.1 (ATP-binding cassette, sub-family C (CFTR/MRP), member 4); canalicular multispecific organic anion transporter (ABC superfamily)
Chromosome: 13; Location: 13q32
Annotation: Chromosome 13, NC_000013.9 (94470090..94751684, complement)
MIM: 605250
GeneID: 10257
66: ABCF2  
Official Symbol ABCF2 and Name: ATP-binding cassette, sub-family F (GCN20), member 2 [Homo sapiens]
Other Aliases: ABC28, DKFZp586K1823, EST133090, HUSSY-18, M-ABC1
Other Designations: ABC-type transport protein; ATP-binding cassette, sub-family F, member 2; Iron inhibited ABC transporter 2
Chromosome: 7; Location: 7q36
Annotation: Chromosome 7, NC_000007.12 (150535856..150555250, complement)
GeneID: 10061
67: ABCB1  
Official Symbol ABCB1 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 1 [Homo sapiens]
Other Aliases: ABC20, CD243, CLCS, GP170, MDR1, MGC163296, P-gp, PGY1
Other Designations: ATP-binding cassette sub-family B member 1; P glycoprotein 1; P-glycoprotein 1; colchicin sensitivity; doxorubicin resistance; multidrug resistance 1
Chromosome: 7; Location: 7q21.1
Annotation: Chromosome 7, NC_000007.12 (86970884..87180500, complement)
MIM: 171050
GeneID: 5243
68: SLC26A7  
Official Symbol SLC26A7 and Name: solute carrier family 26, member 7 [Homo sapiens]
Other Aliases: MGC126268, SUT2
Other Designations: sulfate anion transporter
Chromosome: 8; Location: 8q23
Annotation: Chromosome 8, NC_000008.9 (92330692..92479554)
MIM: 608479
GeneID: 115111
69: LOC146167
similar to amino acid transporter [Homo sapiens]
Other Designations: hypothetical protein LOC146167
Chromosome: 16; Location: 16q23.3
Annotation: Chromosome 16, NC_000016.8 (82600890..82633263, complement)
GeneID: 146167
70: SLCO3A1  
Official Symbol SLCO3A1 and Name: solute carrier organic anion transporter family, member 3A1 [Homo sapiens]
Other Aliases: FLJ40478, OATP-D, OATP3A1, SLC21A11
Other Designations: solute carrier family 21 (organic anion transporter), member 11
Chromosome: 15; Location: 15q26
Annotation: Chromosome 15, NC_000015.8 (90197950..90507783)
GeneID: 28232
71: C19orf28  
Official Symbol C19orf28 and Name: chromosome 19 open reading frame 28 [Homo sapiens]
Other Aliases: MGC20700, PP3501
Other Designations: hypothetical protein LOC126321
Chromosome: 19; Location: 19p13.3
Annotation: Chromosome 19, NC_000019.8 (3495197..3508561, complement)
GeneID: 126321
72: PERF15
lipid-binding protein [Homo sapiens]
Other Designations: hypothetical protein LOC646480
Chromosome: 8; Location: 8q21.13
Annotation: Chromosome 8, NC_000008.9 (82533173..82536313, complement)
GeneID: 646480
73: SLC35C2  
Official Symbol SLC35C2 and Name: solute carrier family 35, member C2 [Homo sapiens]
Other Aliases: RP11-394O2.1, BA394O2.1, C20orf5, CGI-15, FLJ37039, MGC20633, MGC32079, MGC39183, OVCOV1
Other Designations: ovarian cancer overexpressed 1
Chromosome: 20; Location: 20q13.12
Annotation: Chromosome 20, NC_000020.9 (44411584..44426471, complement)
GeneID: 51006
74: SLC26A6  
Official Symbol SLC26A6 and Name: solute carrier family 26, member 6 [Homo sapiens]
Other Aliases: DKFZp586E1422
Other Designations: anion transporter 1; pendrin L1; pendrin-like protein 1; sulfate anion transporter
Chromosome: 3; Location: 3p21.3
Annotation: Chromosome 3, NC_000003.10 (48638160..48647930, complement)
MIM: 610068
GeneID: 65010
75: SLC45A1
Official Symbol SLC45A1 and Name: solute carrier family 45, member 1 [Homo sapiens]
Other Aliases: DNB5, KIAA0458
Other Designations: DNB5; OTTHUMP00000043387; deleted in neuroblastoma 5
Chromosome: 1; Location: 1p36.1-p36.2
Annotation: Chromosome 1, NC_000001.9 (8306977..8326814)
MIM: 605763
GeneID: 50651
76: LOC388931
hypothetical protein LOC388931 [Homo sapiens]
Chromosome: 2; Location: 2p23.3
Annotation: Chromosome 2, NC_000002.10 (24086457..24100649)
GeneID: 388931
77: SLC38A1  
Official Symbol SLC38A1 and Name: solute carrier family 38, member 1 [Homo sapiens]
Other Aliases: ATA1, NAT2, SAT1, SNAT1
Other Designations: amino acid transporter system A1
Chromosome: 12; Location: 12q13.11
Annotation: Chromosome 12, NC_000012.10 (44867833..44948824, complement)
MIM: 608490
GeneID: 81539
78: SLC39A7  
Official Symbol SLC39A7 and Name: solute carrier family 39 (zinc transporter), member 7 [Homo sapiens]
Other Aliases: D6S115E, D6S2244E, H2-KE4, HKE4, KE4, RING5, ZIP7
Other Designations: HLA class II region expressed gene KE4; Ke4 gene, mouse, human homolog of; solute carrier family 39, member 7
Chromosome: 6; Location: 6p21.3
Annotation: Chromosome 6, NC_000006.10 (33276675..33280191)
MIM: 601416
GeneID: 7922
79: SLC41A1
Official Symbol SLC41A1 and Name: solute carrier family 41, member 1 [Homo sapiens]
Other Aliases: MgtE
Other Designations: solute carrier family 41 member 1
Chromosome: 1; Location: 1q32.1
Annotation: Chromosome 1, NC_000001.9 (204024844..204048784, complement)
MIM: 610801
GeneID: 254428
80: ABCC8
Official Symbol ABCC8 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 8 [Homo sapiens]
Other Aliases: ABC36, HHF1, HI, HRINS, MRP8, PHHI, SUR, SUR1, TNDM2
Other Designations: ATP-binding cassette, sub-family C, member 8; sulfonylurea receptor (hyperinsulinemia)
Chromosome: 11; Location: 11p15.1
Annotation: Chromosome 11, NC_000011.8 (17371009..17455025, complement)
MIM: 600509
GeneID: 6833
81: ABCG8  
Official Symbol ABCG8 and Name: ATP-binding cassette, sub-family G (WHITE), member 8 (sterolin 2) [Homo sapiens]
Other Aliases: MGC142217, STSL
Other Designations: ATP-binding cassette, subfamily G, member 8; sterolin 2
Chromosome: 2; Location: 2p21
Annotation: Chromosome 2, NC_000002.10 (43919607..43959109)
MIM: 605460
GeneID: 64241
82: SLC39A6  
Official Symbol SLC39A6 and Name: solute carrier family 39 (zinc transporter), member 6 [Homo sapiens]
Other Aliases: LIV-1
Other Designations: LIV-1 protein, estrogen regulated; solute carrier family 39 (metal ion transporter), member 6
Chromosome: 18; Location: 18q12.2
Annotation: Chromosome 18, NC_000018.8 (31943197..31963203, complement)
MIM: 608731
GeneID: 25800
83: ABCB10  
Official Symbol ABCB10 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 10 [Homo sapiens]
Other Aliases: EST20237, M-ABC2, MTABC2
Other Designations: ATP-binding cassette, sub-family B, member 10
Chromosome: 1; Location: 1q42
Annotation: Chromosome 1, NC_000001.9 (227718953..227761065, complement)
MIM: 605454
GeneID: 23456
84: ABCG4  
Official Symbol ABCG4 and Name: ATP-binding cassette, sub-family G (WHITE), member 4 [Homo sapiens]
Other Aliases: WHITE2
Other Designations: ATP-binding cassette, subfamily G, member 4; putative ABC transporter
Chromosome: 11; Location: 11q23.3
Annotation: Chromosome 11, NC_000011.8 (118524960..118538585)
MIM: 607784
GeneID: 64137
85: ABCB8  
Official Symbol ABCB8 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 8 [Homo sapiens]
Other Aliases: EST328128, M-ABC1, MABC1
Other Designations: ATP-binding cassette, sub-family B, member 8; mitochondrial ABC protein
Chromosome: 7; Location: 7q36
Annotation: Chromosome 7, NC_000007.12 (150356470..150373585)
MIM: 605464
GeneID: 11194
86: ABCB11
Official Symbol ABCB11 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 11 [Homo sapiens]
Other Aliases: ABC16, BSEP, PFIC-2, PFIC2, PGY4, SPGP
Other Designations: ABC member 16, MDR/TAP subfamily; bile salt export pump; progressive familial intrahepatic cholestasis 2; sister p-glycoprotein
Chromosome: 2; Location: 2q24
Annotation: Chromosome 2, NC_000002.10 (169487695..169596079, complement)
MIM: 603201
GeneID: 8647
87: ABCC11
Official Symbol ABCC11 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 11 [Homo sapiens]
Other Aliases: EWWD, MRP8, WW
Other Designations: ATP-binding cassette protein C11; ATP-binding cassette transporter MRP8; ATP-binding cassette, sub-family C, member 11; multi-resistance protein 8
Chromosome: 16; Location: 16q12.1
Annotation: Chromosome 16, NC_000016.8 (46758323..46826589, complement)
MIM: 607040
GeneID: 85320
88: ABCC12  
Official Symbol ABCC12 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 12 [Homo sapiens]
Other Aliases: MGC27071, MRP9
Other Designations: ATP-binding cassette protein C12; ATP-binding cassette transporter sub-family C member 12; multidrug resistance-associated protein 9
Chromosome: 16; Location: 16q12.1
Annotation: Chromosome 16, NC_000016.8 (46674385..46738182, complement)
MIM: 607041
GeneID: 94160
89: ABCB6  
Official Symbol ABCB6 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 6 [Homo sapiens]
Other Aliases: ABC, ABC14, EST45597, FLJ22414, MTABC3, PRP, umat
Other Designations: ATP-binding cassette half-transporter; ATP-binding cassette, sub-family B, member 6
Chromosome: 2; Location: 2q36
Annotation: Chromosome 2, NC_000002.10 (219782738..219791916, complement)
MIM: 605452
GeneID: 10058
90: ABCC6  
Official Symbol ABCC6 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 6 [Homo sapiens]
Other Aliases: ABC34, ARA, EST349056, MLP1, MOATE, MRP6, PXE, PXE1
Other Designations: ATP-binding cassette, sub-family C, member 6; anthracycline resistance associated protein; anthracycline resistance-associated; pseudoxanthoma elasticum
Chromosome: 16; Location: 16p13.1
Annotation: Chromosome 16, NC_000016.8 (16151491..16224815, complement)
MIM: 603234
GeneID: 368
91: ABCA1
Official Symbol ABCA1 and Name: ATP-binding cassette, sub-family A (ABC1), member 1 [Homo sapiens]
Other Aliases: ABC-1, ABC1, CERP, FLJ14958, HDLDT1, TGD
Other Designations: ATP binding cassette transporter 1; ATP-binding cassette 1; ATP-binding cassette transporter-1; ATP-binding cassette, sub-family A member 1; cholesterol efflux regulatory protein; high density lipoprotein deficiency, Tangier type, 1; membrane-bound
Chromosome: 9; Location: 9q31.1
Annotation: Chromosome 9, NC_000009.10 (106583104..106730257, complement)
MIM: 600046
GeneID: 19
92: TAP1  
Official Symbol TAP1 and Name: transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) [Homo sapiens]
Other Aliases: DAQB-69D7.3, ABC17, ABCB2, APT1, D6S114E, FLJ26666, FLJ41500, PSF1, RING4, TAP1*0102N, TAP1N
Other Designations: ABC transporter, MHC 1; ATP-binding cassette transporter; ATP-binding cassette, sub-family B (MDR/TAP), member 2; ATP-binding cassette, sub-family B, member 2; antigen peptide transporter 1; peptide supply factor 1; transporter 1, ATP-binding cassette, sub-family B; transporter associated with antigen processing; transporter, ATP-binding cassette, major histocompatibility complex, 1
Chromosome: 6; Location: 6p21.3
Annotation: Chromosome 6, NC_000006.10 (32920964..32929726, complement)
MIM: 170260
GeneID: 6890
93: SLC1A3  
Official Symbol SLC1A3 and Name: solute carrier family 1 (glial high affinity glutamate transporter), member 3 [Homo sapiens]
Other Aliases: EA6, EAAT1, FLJ25094, GLAST, GLAST1
Other Designations: glutamate transporter variant EAAT1ex9skip
Chromosome: 5; Location: 5p13
Annotation: Chromosome 5, NC_000005.8 (36642446..36724191)
MIM: 600111
GeneID: 6507
94: SLC1A2  
Official Symbol SLC1A2 and Name: solute carrier family 1 (glial high affinity glutamate transporter), member 2 [Homo sapiens]
Other Aliases: EAAT2, GLT-1
Other Designations: excitatory amino acid transporter 2; excitotoxic amino acid transporter 2; glial high affinity glutamate transporter; glutamate/aspartate transporter II; sodium-dependent glutamate/aspartate transporter 2; solute carrier family 1, member 2
Chromosome: 11; Location: 11p13-p12
Annotation: Chromosome 11, NC_000011.8 (35229329..35397372, complement)
MIM: 600300
GeneID: 6506
95: SLC1A1  
Official Symbol SLC1A1 and Name: solute carrier family 1 (neuronal/epithelial high affinity glutamate transporter, system Xag), member 1 [Homo sapiens]
Other Aliases: EAAC1, EAAT3
Other Designations: excitatory amino acid carrier 1; excitatory amino acid transporter-3; solute carrier family 1, member 1
Chromosome: 9; Location: 9p24
Annotation: Chromosome 9, NC_000009.10 (4480444..4577469)
MIM: 133550
GeneID: 6505
96: ABCA10
Official Symbol ABCA10 and Name: ATP-binding cassette, sub-family A (ABC1), member 10 [Homo sapiens]
Other Aliases: EST698739
Other Designations: ATP-binding cassette A10; ATP-binding cassette sub-family A member 10; ATP-binding cassette, sub-family A, member 10
Chromosome: 17; Location: 17q24
Annotation: Chromosome 17, NC_000017.9 (64655744..64752551, complement)
GeneID: 10349
97: ABCC5  
Official Symbol ABCC5 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 5 [Homo sapiens]
Other Aliases: ABC33, DKFZp686C1782, EST277145, MOAT-C, MOATC, MRP5, SMRP, pABC11
Other Designations: ATP-binding cassette, sub-family C, member 5; canalicular multispecific organic anion transporter C
Chromosome: 3; Location: 3q27
Annotation: Chromosome 3, NC_000003.10 (185120416..185218421, complement)
MIM: 605251
GeneID: 10057
98: SLC26A9
Official Symbol SLC26A9 and Name: solute carrier family 26, member 9 [Homo sapiens]
Other Designations: anion transporter/exchanger-9
Chromosome: 1; Location: 1q31-q32
Annotation: Chromosome 1, NC_000001.9 (204148799..204179211, complement)
MIM: 608481
GeneID: 115019
99: MGC15523  
hypothetical protein MGC15523 [Homo sapiens]
Other Aliases: FLJ35718
Other Designations: hypothetical protein LOC124565
Chromosome: 17; Location: 17q25.3
Annotation: Chromosome 17, NC_000017.9 (76833394..76883691, complement)
GeneID: 124565
100: SLC26A2  
Official Symbol SLC26A2 and Name: solute carrier family 26 (sulfate transporter), member 2 [Homo sapiens]
Other Aliases: D5S1708, DTD, DTDST, EDM4, MST153, MSTP157
Other Designations: diastrophic dysplasia sulfate transporter; solute carrier family 26 member 2; sulfate anion transporter 1
Chromosome: 5; Location: 5q31-q34
Annotation: Chromosome 5, NC_000005.8 (149320639..149347156)
MIM: 606718
GeneID: 1836
101: SLCO1A2  
Official Symbol SLCO1A2 and Name: solute carrier organic anion transporter family, member 1A2 [Homo sapiens]
Other Aliases: OATP, OATP-A, OATP1A2, SLC21A3
Other Designations: organic anion transporting polypeptide A; sodium-independent organic anion transporter; solute carrier family 21 (organic anion transporter), member 3
Chromosome: 12; Location: 12p12
Annotation: Chromosome 12, NC_000012.10 (21313094..21439638, complement)
MIM: 602883
GeneID: 6579
102: SLC26A5  
Official Symbol SLC26A5 and Name: solute carrier family 26, member 5 (prestin) [Homo sapiens]
Other Aliases: DFNB61, MGC118886, MGC118887, MGC118888, MGC118889, PRES
Other Designations: deafness, neurosensory, autosomal recessive, 61; prestin; prestin (motor protein)
Chromosome: 7; Location: 7q22.1
Annotation: Chromosome 7, NC_000007.12 (102780413..102873834, complement)
MIM: 604943
GeneID: 375611
103: SLC26A8  
Official Symbol SLC26A8 and Name: solute carrier family 26, member 8 [Homo sapiens]
Other Aliases: RP11-482O9.1, FLJ32714, TAT1
Other Designations: OTTHUMP00000039697; anion transporter/exchanger-8; testis anion transporter 1
Chromosome: 6; Location: 6p21
Annotation: Chromosome 6, NC_000006.10 (36019271..36100355, complement)
MIM: 608480
GeneID: 116369
104: SLC39A3  
Official Symbol SLC39A3 and Name: solute carrier family 39 (zinc transporter), member 3 [Homo sapiens]
Other Aliases: ZIP3
Other Designations: zinc transporter
Chromosome: 19; Location: 19p13.3
Annotation: Chromosome 19, NC_000019.8 (2683522..2691074, complement)
GeneID: 29985
105: SLC26A11  
Official Symbol SLC26A11 and Name: solute carrier family 26, member 11 [Homo sapiens]
Other Aliases: MGC46523
Chromosome: 17; Location: 17q25.3
Annotation: Chromosome 17, NC_000017.9 (75808832..75841892)
MIM: 610117
GeneID: 284129
106: SLC9A6  
Official Symbol SLC9A6 and Name: solute carrier family 9 (sodium/hydrogen exchanger), member 6 [Homo sapiens]
Other Aliases: RP11-274K13.1, KIAA0267, NHE6
Other Designations: solute carrier family 9 (sodium/hydrogen exchanger), isoform 6
Chromosome: X; Location: Xq26.3
Annotation: Chromosome X, NC_000023.9 (134895293..134956958)
MIM: 300231
GeneID: 10479
107: SLC45A2  
Official Symbol SLC45A2 and Name: solute carrier family 45, member 2 [Homo sapiens]
Other Aliases: 1A1, AIM1, MATP
Other Designations: melanoma antigen AIM1; membrane associated transporter; membrane-associated transporter protein; underwhite
Chromosome: 5; Location: 5p13.3
Annotation: Chromosome 5, NC_000005.8 (33980478..34020537, complement)
MIM: 606202
GeneID: 51151
108: SLC35B1  
Official Symbol SLC35B1 and Name: solute carrier family 35, member B1 [Homo sapiens]
Other Aliases: UGTREL1
Other Designations: UDP-galactose transporter related
Chromosome: 17; Location: 17q21.33
Annotation: Chromosome 17, NC_000017.9 (45133689..45140281, complement)
MIM: 610790
GeneID: 10237
109: RAD50
Official Symbol RAD50 and Name: RAD50 homolog (S. cerevisiae) [Homo sapiens]
Other Aliases: RAD50-2, hRad50
Other Designations: RAD50 homolog
Chromosome: 5; Location: 5q31
Annotation: Chromosome 5, NC_000005.8 (131920529..132007498)
MIM: 604040
GeneID: 10111
110: SLC39A4  
Official Symbol SLC39A4 and Name: solute carrier family 39 (zinc transporter), member 4 [Homo sapiens]
Other Aliases: AEZ, FLJ20327, MGC74741, ZIP4
Other Designations: acrodermatitis enteropathica, zinc-deficiency type; zinc transporter ZIP4
Chromosome: 8; Location: 8q24.3
Annotation: Chromosome 8, NC_000008.9 (145608606..145613081, complement)
MIM: 607059
GeneID: 55630
111: PAEP  
Official Symbol PAEP and Name: progestagen-associated endometrial protein (placental protein 14, pregnancy-associated endometrial alpha-2-globulin, alpha uterine protein) [Homo sapiens]
Other Aliases: GD, GdA, GdF, GdS, MGC138509, MGC142288, PAEG, PEP, PP14
Other Designations: glycodelin; glycodelin-A; glycodelin-F; glycodelin-S; progesterone-associated endometrial protein
Chromosome: 9; Location: 9q34
Annotation: Chromosome 9, NC_000009.10 (137593425..137598443)
MIM: 173310
GeneID: 5047
112: SLC41A2  
Official Symbol SLC41A2 and Name: solute carrier family 41, member 2 [Homo sapiens]
Other Aliases: DKFZP434K0427, MGC125330, MGC125331, SLC41A1-L1
Other Designations: SLC41A1-like 1
Chromosome: 12; Location: 12q23.3
Annotation: Chromosome 12, NC_000012.10 (103722491..103846562, complement)
MIM: 610802
GeneID: 84102
113: SLC39A10  
Official Symbol SLC39A10 and Name: solute carrier family 39 (zinc transporter), member 10 [Homo sapiens]
Other Aliases: DKFZp781L10106, LZT-Hs2, MGC126565, MGC138428
Other Designations: solute carrier family 39 (metal ion transporter), member 10
Chromosome: 2; Location: 2q32.3
Annotation: Chromosome 2, NC_000002.10 (196230184..196310663)
MIM: 608733
GeneID: 57181
114: ABCB5  
Official Symbol ABCB5 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 5 [Homo sapiens]
Other Aliases: ABCB5alpha, ABCB5beta, EST422562
Other Designations: ATP-binding cassette, sub-family B, member 5; P-glycoprotein ABCB5
Chromosome: 7; Location: 7p15.3
Annotation: Chromosome 7, NC_000007.12 (20653570..20761772)
GeneID: 340273
115: SLC26A3  
Official Symbol SLC26A3 and Name: solute carrier family 26, member 3 [Homo sapiens]
Other Aliases: CLD, DRA
Other Designations: congenital chloride diarrhea; down-regulated in adenoma; down-regulated in adenoma protein
Chromosome: 7; Location: 7q31
Annotation: Chromosome 7, NC_000007.12 (107193153..107230873, complement)
MIM: 126650
GeneID: 1811
116: SLC39A8  
Official Symbol SLC39A8 and Name: solute carrier family 39 (zinc transporter), member 8 [Homo sapiens]
Other Aliases: BIGM103, LZT-Hs6
Other Designations: solute carrier family 39 (metal ion transporter), member 8; up-regulated by BCG-CWS
Chromosome: 4; Location: 4q22-q24
Annotation: Chromosome 4, NC_000004.10 (103401844..103485371, complement)
MIM: 608732
GeneID: 64116
117: SLC35D2  
Official Symbol SLC35D2 and Name: solute carrier family 35, member D2 [Homo sapiens]
Other Aliases: HFRC1, MGC117215, MGC142139, SQV7L, UGTrel8, hfrc
Other Designations: UDP-N-acetylglucosamine transporter; fringe connection
Chromosome: 9; Location: 9q22.32
Annotation: Chromosome 9, NC_000009.10 (98122809..98185758, complement)
MIM: 609182
GeneID: 11046
118: SLC7A5  
Official Symbol SLC7A5 and Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 5 [Homo sapiens]
Other Aliases: 4F2LC, CD98, D16S469E, E16, LAT1, MPE16, hLAT1
Other Designations: 4F2 light chain; CD98 light chain; L-type amino acid transporter 1; integral membrane protein E16; large neutral amino acids transporter 1; large neutral amino acids transporter small subunit 1; sodium-independent neutral amino acid transporter LAT1
Chromosome: 16; Location: 16q24.3
Annotation: Chromosome 16, NC_000016.8 (86421130..86460601, complement)
MIM: 600182
GeneID: 8140
119: SLC26A4  
Official Symbol SLC26A4 and Name: solute carrier family 26, member 4 [Homo sapiens]
Other Aliases: DFNB4, PDS
Other Designations: pendrin
Chromosome: 7; Location: 7q31
Annotation: Chromosome 7, NC_000007.12 (107088316..107145490)
MIM: 605646
GeneID: 5172
120: SLC39A5  
Official Symbol SLC39A5 and Name: solute carrier family 39 (metal ion transporter), member 5 [Homo sapiens]
Other Aliases: LZT-Hs7, MGC34778, ZIP5
Chromosome: 12; Location: 12q13.2
Annotation: Chromosome 12, NC_000012.10 (54910894..54917897)
MIM: 608730
GeneID: 283375
121: SLC39A13  
Official Symbol SLC39A13 and Name: solute carrier family 39 (zinc transporter), member 13 [Homo sapiens]
Other Aliases: FLJ25785
Other Designations: solute carrier family 39 (metal ion transporter), member 13
Chromosome: 11; Location: 11p11.2
Annotation: Chromosome 11, NC_000011.8 (47386758..47394623)
MIM: 608735
GeneID: 91252
122: ABCA12
Official Symbol ABCA12 and Name: ATP-binding cassette, sub-family A (ABC1), member 12 [Homo sapiens]
Other Aliases: DKFZp434G232, FLJ41584, ICR2B, LI2
Other Designations: ATP-binding cassette, sub-family A, member 12
Chromosome: 2; Location: 2q34
Annotation: Chromosome 2, NC_000002.10 (215504511..215711396, complement)
MIM: 607800
GeneID: 26154
123: SLC22A8  
Official Symbol SLC22A8 and Name: solute carrier family 22 (organic anion transporter), member 8 [Homo sapiens]
Other Aliases: MGC24086, OAT3
Other Designations: organic anion transporter 3; solute carrier family 22 member 8
Chromosome: 11; Location: 11q11
Annotation: Chromosome 11, NC_000011.8 (62516872..62539887, complement)
MIM: 607581
GeneID: 9376
124: SLC22A6  
Official Symbol SLC22A6 and Name: solute carrier family 22 (organic anion transporter), member 6 [Homo sapiens]
Other Aliases: HOAT1, MGC45260, OAT1, PAHT, ROAT1
Other Designations: para-aminohippurate transporter; renal organic anion transporter 1; solute carrier family 22 member 6
Chromosome: 11; Location: 11q13.1-q13.2
Annotation: Chromosome 11, NC_000011.8 (62500645..62509045, complement)
MIM: 607582
GeneID: 9356
125: ABCA5
Official Symbol ABCA5 and Name: ATP-binding cassette, sub-family A (ABC1), member 5 [Homo sapiens]
Other Aliases: ABC13, DKFZp451F117, DKFZp779N2435, EST90625, FLJ16381
Other Designations: ATP-binding cassette A5; ATP-binding cassette, sub-family A , member 5
Chromosome: 17; Location: 17q24.3
Annotation: Chromosome 17, NC_000017.9 (64754386..64834885, complement)
GeneID: 23461
126: ABCA6  
Official Symbol ABCA6 and Name: ATP-binding cassette, sub-family A (ABC1), member 6 [Homo sapiens]
Other Aliases: EST155051, FLJ43498
Other Designations: ABC transporter ABCA6; ATP-binding cassette A6; ATP-binding cassette, sub-family A, member 6
Chromosome: 17; Location: 17q24.3
Annotation: Chromosome 17, NC_000017.9 (64586442..64649610, complement)
GeneID: 23460
127: ABCB9  
Official Symbol ABCB9 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 9 [Homo sapiens]
Other Aliases: EST122234, KIAA1520, TAPL
Chromosome: 12; Location: 12q24
Annotation: Chromosome 12, NC_000012.10 (121979492..122025705, complement)
MIM: 605453
GeneID: 23457
128: SLC22A2  
Official Symbol SLC22A2 and Name: solute carrier family 22 (organic cation transporter), member 2 [Homo sapiens]
Other Aliases: MGC32628, OCT2
Other Designations: organic cation transporter (OCT2); organic cation transporter 2; solute carrier family 22 member 2
Chromosome: 6; Location: 6q26
Annotation: Chromosome 6, NC_000006.10 (160557780..160599949, complement)
MIM: 602608
GeneID: 6582
129: SLC22A1  
Official Symbol SLC22A1 and Name: solute carrier family 22 (organic cation transporter), member 1 [Homo sapiens]
Other Aliases: HOCT1, OCT1, oct1_cds
Other Designations: organic cation transporter 1; solute carrier family 22 member 1
Chromosome: 6; Location: 6q26
Annotation: Chromosome 6, NC_000006.10 (160462853..160499740)
MIM: 602607
GeneID: 6580
130: SLC6A4  
Official Symbol SLC6A4 and Name: solute carrier family 6 (neurotransmitter transporter, serotonin), member 4 [Homo sapiens]
Other Aliases: 5-HTT, 5HTT, HTT, OCD1, SERT, hSERT
Other Designations: 5-hydroxytryptamine transporter; 5HT transporter; Na+/Cl- dependent serotonin transporter; serotonin transporter; sodium-dependent serotonin transporter; solute carrier family 6 member 4
Chromosome: 17; Location: 17q11.1-q12
Annotation: Chromosome 17, NC_000017.9 (25549032..25586831, complement)
MIM: 182138
GeneID: 6532
131: SLC2A1  
Official Symbol SLC2A1 and Name: solute carrier family 2 (facilitated glucose transporter), member 1 [Homo sapiens]
Other Aliases: GLUT, GLUT1, MGC141895, MGC141896
Chromosome: 1; Location: 1p35-p31.3
Annotation: Chromosome 1, NC_000001.9 (43164102..43197088, complement)
MIM: 138140
GeneID: 6513
132: ABCC3
Official Symbol ABCC3 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 3 [Homo sapiens]
Other Aliases: ABC31, EST90757, MLP2, MOAT-D, MRP3, cMOAT2
Other Designations: ATP-binding cassette, sub-family C, member 3; canicular multispecific organic anion transporter; multidrug resistance associated protein
Chromosome: 17; Location: 17q22
Annotation: Chromosome 17, NC_000017.9 (46067227..46124062)
MIM: 604323
GeneID: 8714
133: SLC22A16  
Official Symbol SLC22A16 and Name: solute carrier family 22 (organic cation transporter), member 16 [Homo sapiens]
Other Aliases: RP1-261K5.1, CT2, FLIPT2, OCT6, OKB1, dJ261K5.1
Other Designations: OTTHUMP00000040478; WUGSC:RG331P03.1; carnitine transporter 2; fly-like putative organic ion transporter 2; organic cation transporter 6; solute carrier family 22, member 16
Chromosome: 6; Location: 6q21-q22.1
Annotation: Chromosome 6, NC_000006.10 (110852599..110904537, complement)
MIM: 608276
GeneID: 85413
134: ABCC2
Official Symbol ABCC2 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 2 [Homo sapiens]
Other Aliases: ABC30, CMOAT, DJS, KIAA1010, MRP2, cMRP
Other Designations: canalicular multispecific organic anion transporter
Chromosome: 10; Location: 10q24
Annotation: Chromosome 10, NC_000010.9 (101532561..101601571)
MIM: 601107
GeneID: 1244
135: ABCA13
Official Symbol ABCA13 and Name: ATP-binding cassette, sub-family A (ABC1), member 13 [Homo sapiens]
Other Aliases: DKFZp313D2411, FLJ16398, FLJ33876, FLJ33951
Other Designations: ATP binding cassette transporter A13; ATP binding cassette, sub-family A (ABC1), member 13
Chromosome: 7; Location: 7p12.3
Annotation: Chromosome 7, NC_000007.12 (48208389..48657637)
MIM: 607807
GeneID: 154664
136: ABCC10
Official Symbol ABCC10 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 10 [Homo sapiens]
Other Aliases: EST182763, MRP7, SIMRP7
Other Designations: ATP-binding cassette, sub-family C, member 10; multidrug resistance-associated protein 7
Chromosome: 6; Location: 6p21.1
Annotation: Chromosome 6, NC_000006.10 (43507467..43526141)
GeneID: 89845
137: CFTR
Official Symbol CFTR and Name: cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7) [Homo sapiens]
Other Aliases: tcag7.78, ABC35, ABCC7, CF, CFTR/MRP, MRP7, TNR-CFTR, dJ760C5.1
Other Designations: ATP-binding cassette sub-family C, member 7; cystic fibrosis transmembrane conductance regulator
Chromosome: 7; Location: 7q31.2
Annotation: Chromosome 7, NC_000007.12 (116907253..117095955)
MIM: 602421
GeneID: 1080
138: SLC14A2  
Official Symbol SLC14A2 and Name: solute carrier family 14 (urea transporter), member 2 [Homo sapiens]
Other Aliases: FLJ16167, HUT2, MGC119566, MGC119567, UT-A2, UT2, UTR, hUT-A6
Other Designations: Urea transporter-2
Chromosome: 18; Location: 18q12.1-q21.1
Annotation: Chromosome 18, NC_000018.8 (41448764..41517070)
MIM: 601611
GeneID: 8170
139: ABCA8  
Official Symbol ABCA8 and Name: ATP-binding cassette, sub-family A (ABC1), member 8 [Homo sapiens]
Other Aliases: KIAA0822, MGC163152
Other Designations: ATP-binding cassette, sub-family A member 8
Chromosome: 17; Location: 17q24
Annotation: Chromosome 17, NC_000017.9 (64375025..64463128, complement)
GeneID: 10351
140: ABCA9
Official Symbol ABCA9 and Name: ATP-binding cassette, sub-family A (ABC1), member 9 [Homo sapiens]
Other Aliases: DKFZp686F2450, EST640918, MGC75415
Other Designations: ATP-binding cassette A9; ATP-binding cassette, sub-family A, member 9
Chromosome: 17; Location: 17q24.2
Annotation: Chromosome 17, NC_000017.9 (64482368..64568731, complement)
GeneID: 10350
141: BSG  
Official Symbol BSG and Name: basigin (Ok blood group) [Homo sapiens]
Other Aliases: 5F7, CD147, M6, OK, TCSF
Other Designations: M6 antigen; OK blood group; basigin; collagenase stimulatory factor; emmprin; extracellular matrix metalloproteinase inducer
Chromosome: 19; Location: 19p13.3
Annotation: Chromosome 19, NC_000019.8 (522325..534493)
MIM: 109480
GeneID: 682
142: SLC22A15  
Official Symbol SLC22A15 and Name: solute carrier family 22 (organic cation transporter), member 15 [Homo sapiens]
Other Aliases: DKFZp761G0313, FLIPT1, PRO34686
Other Designations: fly-like putative organic ion transporter 1; trans-like protein
Chromosome: 1; Location: 1p13.1
Annotation: Chromosome 1, NC_000001.9 (116320642..116413548)
MIM: 608275
GeneID: 55356
143: ABCB7  
Official Symbol ABCB7 and Name: ATP-binding cassette, sub-family B (MDR/TAP), member 7 [Homo sapiens]
Other Aliases: ABC7, ASAT, Atm1p, EST140535
Other Designations: ATP-binding cassette 7; ATP-binding cassette, sub-family B, member 7; Anemia, sideroblastic, with spinocerebellar ataxia
Chromosome: X; Location: Xq12-q13
Annotation: Chromosome X, NC_000023.9 (74189830..74292857, complement)
MIM: 300135
GeneID: 22
144: ABCF3  
Official Symbol ABCF3 and Name: ATP-binding cassette, sub-family F (GCN20), member 3 [Homo sapiens]
Other Aliases: EST201864, FLJ11198
Chromosome: 3; Location: 3q27.1
Annotation: Chromosome 3, NC_000003.10 (185386580..185394487)
GeneID: 55324
145: SLC36A1  
Official Symbol SLC36A1 and Name: solute carrier family 36 (proton/amino acid symporter), member 1 [Homo sapiens]
Other Aliases: LYAAT1, PAT1, TRAMD3
Other Designations: lysosomal amino acid transporter 1; proton-coupled amino acid transporter; proton/amino acid transporter 1; solute carrier family 36 member 1
Chromosome: 5; Location: 5q33.1
Annotation: Chromosome 5, NC_000005.8 (150807356..150852133)
MIM: 606561
GeneID: 206358
146: MFSD1  
Official Symbol MFSD1 and Name: major facilitator superfamily domain containing 1 [Homo sapiens]
Other Aliases: FLJ14153, UG0581B09
Chromosome: 3; Location: 3q25.33
Annotation: Chromosome 3, NC_000003.10 (160002606..160030198)
GeneID: 64747
147: NMRAL1  
Official Symbol NMRAL1 and Name: NmrA-like family domain containing 1 [Homo sapiens]
Other Aliases: FLJ25918, HSCARG
Chromosome: 16; Location: 16p13.3
Annotation: Chromosome 16, NC_000016.8 (4451696..4464893, complement)
GeneID: 57407
148: SLC38A4  
Official Symbol SLC38A4 and Name: solute carrier family 38, member 4 [Homo sapiens]
Other Aliases: ATA3, FLJ10191, MGC126876, NAT3, PAAT
Other Designations: N amino acid transporter 3; amino acid transporter system A3
Chromosome: 12; Location: 12q13
Annotation: Chromosome 12, NC_000012.10 (45444811..45506006, complement)
MIM: 608065
GeneID: 55089
149: TMCO3  
Official Symbol TMCO3 and Name: transmembrane and coiled-coil domains 3 [Homo sapiens]
Other Aliases: RP11-230F18.3, C13orf11, FLJ20623
Other Designations: B230339H12Rik; OTTHUMP00000040667
Chromosome: 13; Location: 13q34
Annotation: Chromosome 13, NC_000013.9 (113193311..113252508)
GeneID: 55002
150: SLC35B2  
Official Symbol SLC35B2 and Name: solute carrier family 35, member B2 [Homo sapiens]
Other Aliases: RP1-302G2.3, PAPST1, SLL, UGTrel4
Other Designations: 3'-phosphoadenosine 5'-phosphosulfate transporter; OTTHUMP00000016513; OTTHUMP00000016514; OTTHUMP00000039875; solute carrier family 35 member B2 variant 2
Chromosome: 6; Location: 6p12.1-p11.2
Annotation: Chromosome 6, NC_000006.10 (44329821..44333250, complement)
MIM: 610788
GeneID: 347734
151: RBP5  
Official Symbol RBP5 and Name: retinol binding protein 5, cellular [Homo sapiens]
Other Aliases: CRBP-III, CRBP3, CRBPIII
Other Designations: putative cellular retinol-binding protein CRBP III; retinol-binding protein 5, cellular
Chromosome: 12; Location: 12p13.31
Annotation: Chromosome 12, NC_000012.10 (7167554..7172733, complement)
GeneID: 83758
152: FABP7  
Official Symbol FABP7 and Name: fatty acid binding protein 7, brain [Homo sapiens]
Other Aliases: B-FABP, BLBP, DKFZp547J2313, FABPB, MRG
Other Designations: brain lipid binding protein; mammary-derived growth inhibitor-related
Chromosome: 6; Location: 6q22-q23
Annotation: Chromosome 6, NC_000006.10 (123142345..123146918)
MIM: 602965
GeneID: 2173
153: FABP5  
Official Symbol FABP5 and Name: fatty acid binding protein 5 (psoriasis-associated) [Homo sapiens]
Other Aliases: E-FABP, EFABP, PA-FABP, PAFABP
Chromosome: 8; Location: 8q21.13
Annotation: Chromosome 8, NC_000008.9 (82355340..82359563)
MIM: 605168
GeneID: 2171
154: FABP3  
Official Symbol FABP3 and Name: fatty acid binding protein 3, muscle and heart (mammary-derived growth inhibitor) [Homo sapiens]
Other Aliases: FABP11, H-FABP, MDGI, O-FABP
Other Designations: Fatty acid-binding protein 3, muscle; fatty acid binding protein 11; fatty acid binding protein 3; mammary-derived growth inhibitor
Chromosome: 1; Location: 1p33-p32
Annotation: Chromosome 1, NC_000001.9 (31610687..31618510, complement)
MIM: 134651
GeneID: 2170
155: FABP1  
Official Symbol FABP1 and Name: fatty acid binding protein 1, liver [Homo sapiens]
Other Aliases: FABPL, L-FABP
Other Designations: Fatty acid-binding protein, liver
Chromosome: 2; Location: 2p11
Annotation: Chromosome 2, NC_000002.10 (88203625..88208693, complement)
MIM: 134650
GeneID: 2168
156: FABP4  
Official Symbol FABP4 and Name: fatty acid binding protein 4, adipocyte [Homo sapiens]
Other Aliases: A-FABP
Chromosome: 8; Location: 8q21
Annotation: Chromosome 8, NC_000008.9 (82553481..82558004, complement)
MIM: 600434
GeneID: 2167
157: SLC39A11  
Official Symbol SLC39A11 and Name: solute carrier family 39 (metal ion transporter), member 11 [Homo sapiens]
Other Aliases: C17orf26
Chromosome: 17; Location: 17q24.3-q25.1
Annotation: Chromosome 17, NC_000017.9 (68153683..68600427, complement)
GeneID: 201266
158: LCN6  
Official Symbol LCN6 and Name: lipocalin 6 [Homo sapiens]
Other Aliases: LCN5, UNQ643, hLcn5
Other Designations: epididymal-specific lipocalin LCN6; lipocalin 5
Chromosome: 9; Location: 9q34.3
Annotation: Chromosome 9, NC_000009.10 (138758290..138762801, complement)
MIM: 609379
GeneID: 158062
159: SLC36A2  
Official Symbol SLC36A2 and Name: solute carrier family 36 (proton/amino acid symporter), member 2 [Homo sapiens]
Other Aliases: FLJ16051, MGC119658, MGC119660, PAT2, TRAMD1
Other Designations: proton/amino acid transporter 2; tramdorin
Chromosome: 5; Location: 5q33.1
Annotation: Chromosome 5, NC_000005.8 (150674732..150707312, complement)
MIM: 608331
GeneID: 153201
160: FLJ90709  
hypothetical protein FLJ90709 [Homo sapiens]
Other Aliases: FLJ46104, MGC120544
Other Designations: hypothetical protein LOC153129
Chromosome: 5; Location: 5q11.2
Annotation: Chromosome 5, NC_000005.8 (54957435..55043852, complement)
GeneID: 153129
161: SLCO1B3  
Official Symbol SLCO1B3 and Name: solute carrier organic anion transporter family, member 1B3 [Homo sapiens]
Other Aliases: LST-3TM13, LST3, OATP1B3, OATP8, SLC21A8
Other Designations: liver-specific organic anion transporter 3TM13; organic anion transporter LST-3c; solute carrier family 21 (organic anion transporter), member 8
Chromosome: 12; Location: 12p12
Annotation: Chromosome 12, NC_000012.10 (20859895..20960925)
MIM: 605495
GeneID: 28234
162: SLCO4A1  
Official Symbol SLCO4A1 and Name: solute carrier organic anion transporter family, member 4A1 [Homo sapiens]
Other Aliases: OATP-E, OATP1, OATP4A1, OATPRP1, POAT, SLC21A12
Other Designations: colon organic anion transporter; organic anion transporter polypeptide-related protein 1; organic anion transporting polypeptide E; sodium-independent organic anion transporter E; solute carrier family 21 (organic anion transporter), member 12; solute carrier family 21 member 12; solute carrier organic anion transporter family member 4A1
Chromosome: 20; Location: 20q13.33
Annotation: Chromosome 20, NC_000020.9 (60744242..60774092)
GeneID: 28231
163: SLC13A2  
Official Symbol SLC13A2 and Name: solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2 [Homo sapiens]
Other Aliases: NADC1, NaDC-1
Chromosome: 17; Location: 17p13.2
Annotation: Chromosome 17, NC_000017.9 (23824791..23848514)
MIM: 604148
GeneID: 9058
164: SLC7A6  
Official Symbol SLC7A6 and Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 6 [Homo sapiens]
Other Aliases: DKFZp686K15246, KIAA0245, LAT-2, LAT3, y+LAT-2
Other Designations: amino acid permease
Chromosome: 16; Location: 16q22.1
Annotation: Chromosome 16, NC_000016.8 (66855934..66893222)
MIM: 605641
GeneID: 9057
165: SLC7A7  
Official Symbol SLC7A7 and Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 7 [Homo sapiens]
Other Aliases: LAT3, LPI, Y+LAT1, y+LAT-1
Chromosome: 14; Location: 14q11.2
Annotation: Chromosome 14, NC_000014.7 (22312274..22354852, complement)
MIM: 603593
GeneID: 9056
166: SLC35D3  
Official Symbol SLC35D3 and Name: solute carrier family 35, member D3 [Homo sapiens]
Other Aliases: FRCL1, MGC102873, bA55K22.3
Other Designations: frc, fringe-like 1
Chromosome: 6; Location: 6q23.3
Annotation: Chromosome 6, NC_000006.10 (137285095..137288470)
GeneID: 340146
167: SLC7A13  
Official Symbol SLC7A13 and Name: solute carrier family 7, (cationic amino acid transporter, y+ system) member 13 [Homo sapiens]
Other Aliases: AGT-1, AGT1, MGC150476, MGC150477, XAT2
Other Designations: amino acid transporter XAT2
Chromosome: 8; Location: 8q21.3
Annotation: Chromosome 8, NC_000008.9 (87295404..87311720, complement)
GeneID: 157724
168: SLCO2B1  
Official Symbol SLCO2B1 and Name: solute carrier organic anion transporter family, member 2B1 [Homo sapiens]
Other Aliases: DKFZp686E0517, KIAA0880, OATP-B, OATP2B1, OATPB, SLC21A9
Other Designations: solute carrier family 21 (organic anion transporter), member 9
Chromosome: 11; Location: 11q13
Annotation: Chromosome 11, NC_000011.8 (74539811..74594947)
MIM: 604988
GeneID: 11309
169: SLCO2A1  
Official Symbol SLCO2A1 and Name: solute carrier organic anion transporter family, member 2A1 [Homo sapiens]
Other Aliases: OATP2A1, PGT, SLC21A2
Other Designations: solute carrier family 21 (prostaglandin transporter), member 2
Chromosome: 3; Location: 3q21
Annotation: Chromosome 3, NC_000003.10 (135134230..135231418, complement)
MIM: 601460
GeneID: 6578
170: SLC15A2  
Official Symbol SLC15A2 and Name: solute carrier family 15 (H+/peptide transporter), member 2 [Homo sapiens]
Other Aliases: PEPT2
Chromosome: 3; Location: 3q13.33
Annotation: Chromosome 3, NC_000003.10 (123095977..123143148)
MIM: 602339
GeneID: 6565
171: SLC15A1  
Official Symbol SLC15A1 and Name: solute carrier family 15 (oligopeptide transporter), member 1 [Homo sapiens]
Other Aliases: HPECT1, HPEPT1, PEPT1
Other Designations: bA551M18.1.1 (solute carrier family 15 (oligopeptide transporter) member 1); peptide transporter HPEPT1
Chromosome: 13; Location: 13q33-q34
Annotation: Chromosome 13, NC_000013.9 (98134057..98202909, complement)
MIM: 600544
GeneID: 6564
172: SLC10A1  
Official Symbol SLC10A1 and Name: solute carrier family 10 (sodium/bile acid cotransporter family), member 1 [Homo sapiens]
Other Aliases: NTCP, NTCP1
Other Designations: growth-inhibiting protein 29; sodium-dependent taurocholate cotransporter; sodium/bile acid cotransporter
Chromosome: 14; Location: 14q24.1
Annotation: Chromosome 14, NC_000014.7 (69312305..69333707, complement)
MIM: 182396
GeneID: 6554
173: SLC9A5  
Official Symbol SLC9A5 and Name: solute carrier family 9 (sodium/hydrogen exchanger), member 5 [Homo sapiens]
Other Aliases: NHE5
Other Designations: solute carrier family 9 (sodium/hydrogen exchanger), isoform 5
Chromosome: 16; Location: 16q22.1
Annotation: Chromosome 16, NC_000016.8 (65840365..65863595)
MIM: 600477
GeneID: 6553
174: SLC9A3  
Official Symbol SLC9A3 and Name: solute carrier family 9 (sodium/hydrogen exchanger), member 3 [Homo sapiens]
Other Aliases: MGC126718, MGC126720, NHE3
Other Designations: solute carrier family 9 (sodium/hydrogen exchanger), isoform 3
Chromosome: 5; Location: 5p15.3
Annotation: Chromosome 5, NC_000005.8 (526425..577447, complement)
MIM: 182307
GeneID: 6550
175: SLC9A2
Official Symbol SLC9A2 and Name: solute carrier family 9 (sodium/hydrogen exchanger), member 2 [Homo sapiens]
Other Aliases: NHE2
Other Designations: solute carrier family 9 (sodium/hydrogen exchanger), isoform 2
Chromosome: 2; Location: 2q11.2
Annotation: Chromosome 2, NC_000002.10 (102602598..102694241)
MIM: 600530
GeneID: 6549
176: SLC9A1  
Official Symbol SLC9A1 and Name: solute carrier family 9 (sodium/hydrogen exchanger), member 1 (antiporter, Na+/H+, amiloride sensitive) [Homo sapiens]
Other Aliases: APNH, FLJ42224, NHE1
Other Designations: Na+/H+ antiporter, amiloride-sensitive; Na-Li countertransporter; sodium/hydrogen exchanger 1; solute carrier family 9 (sodium/hydrogen exchanger), isoform 1 (antiporter, Na+/H+, amiloride sensitive); solute carrier family 9, isoform A1
Chromosome: 1; Location: 1p36.1-p35
Annotation: Chromosome 1, NC_000001.9 (27297894..27353990, complement)
MIM: 107310
GeneID: 6548
177: SLC38A2  
Official Symbol SLC38A2 and Name: solute carrier family 38, member 2 [Homo sapiens]
Other Aliases: ATA2, KIAA1382, PRO1068, SAT2, SNAT2
Other Designations: amino acid transporter 2; system A amino acid transporter
Chromosome: 12; Location: 12q
Annotation: Chromosome 12, NC_000012.10 (45038238..45052814, complement)
MIM: 605180
GeneID: 54407
178: LCN8  
Official Symbol LCN8 and Name: lipocalin 8 [Homo sapiens]
Other Aliases: EP17, LCN5
Other Designations: OTTHUMP00000022602; lipocalin 5
Chromosome: 9; Location: 9q34.3
Annotation: Chromosome 9, NC_000009.10 (138768661..138772552, complement)
GeneID: 138307
179: SLC38A5  
Official Symbol SLC38A5 and Name: solute carrier family 38, member 5 [Homo sapiens]
Other Aliases: JM24, SN2, pp7194
Other Designations: amino acid transport system N2
Chromosome: X; Location: Xp11.23
Annotation: Chromosome X, NC_000023.9 (48201871..48213509, complement)
MIM: 300649
GeneID: 92745
180: SLC35D1  
Official Symbol SLC35D1 and Name: solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter), member D1 [Homo sapiens]
Other Aliases: KIAA0260, MGC138236, UGTREL7
Other Designations: UDP-glucuronic acid/UDP-N-acetylgalactosamine dual transporter
Chromosome: 1; Location: 1p32-p31
Annotation: Chromosome 1, NC_000001.9 (67242439..67292316, complement)
MIM: 610804
GeneID: 23169
181: LCN2  
Official Symbol LCN2 and Name: lipocalin 2 (oncogene 24p3) [Homo sapiens]
Other Aliases: NGAL
Other Designations: lipocalin 2
Chromosome: 9; Location: 9q34
Annotation: Chromosome 9, NC_000009.10 (129951539..129956333)
MIM: 600181
GeneID: 3934
182: LCN1  
Official Symbol LCN1 and Name: lipocalin 1 (tear prealbumin) [Homo sapiens]
Other Aliases: MGC71975, PMFA, TP, VEGP
Other Designations: Von Ebner gland protein; lipocalin 1; lipocalin 1 (protein migrating faster than albumin, tear prealbumin); lipocalin 1-like 2; tear lipocalin
Chromosome: 9; Location: 9q34
Annotation: Chromosome 9, NC_000009.10 (137553107..137558199)
MIM: 151675
GeneID: 3933
183: SLC32A1  
Official Symbol SLC32A1 and Name: solute carrier family 32 (GABA vesicular transporter), member 1 [Homo sapiens]
Other Aliases: VGAT, VIAAT
Other Designations: GABA and glycine transporter; solute carrier family 32, member 1; vesicular GABA transporter; vesicular inhibitory amino acid transporter
Chromosome: 20; Location: 20q11.23
Annotation: Chromosome 20, NC_000020.9 (36786519..36791429)
GeneID: 140679
184: SLCO6A1  
Official Symbol SLCO6A1 and Name: solute carrier organic anion transporter family, member 6A1 [Homo sapiens]
Other Aliases: GST, MGC26949, OATP6A1, OATPY
Other Designations: gonad-specific transporter; testis-specific organic anion transporter
Chromosome: 5; Location: 5q21.1
Annotation: Chromosome 5, NC_000005.8 (101735550..101862619, complement)
GeneID: 133482
185: SLC38A6  
Official Symbol SLC38A6 and Name: solute carrier family 38, member 6 [Homo sapiens]
Other Aliases: MGC102697, NAT-1
Other Designations: N system amino acid transporter NAT-1
Chromosome: 14; Location: 14q23.1
Annotation: Chromosome 14, NC_000014.7 (60517633..60588929)
GeneID: 145389
186: SLC38A3  
Official Symbol SLC38A3 and Name: solute carrier family 38, member 3 [Homo sapiens]
Other Aliases: G17, SN1
Other Designations: system N1 Na+ and H+-coupled glutamine transporter
Chromosome: 3; Location: 3p21.3
Annotation: Chromosome 3, NC_000003.10 (50217709..50233408)
MIM: 604437
GeneID: 10991
187: CRABP2  
Official Symbol CRABP2 and Name: cellular retinoic acid binding protein 2 [Homo sapiens]
Other Aliases: CRABP-II, RBP6
Other Designations: cellular retinoic acid-binding protein 2
Chromosome: 1; Location: 1q21.3
Annotation: Chromosome 1, NC_000001.9 (154936027..154941999, complement)
MIM: 180231
GeneID: 1382
188: CRABP1  
Official Symbol CRABP1 and Name: cellular retinoic acid binding protein 1 [Homo sapiens]
Other Aliases: CRABP, CRABP-I, CRABPI, RBP5
Other Designations: cellular retinoic acid-binding protein 1
Chromosome: 15; Location: 15q24
Annotation: Chromosome 15, NC_000015.8 (76419750..76427622)
MIM: 180230
GeneID: 1381
189: SLC15A4  
Official Symbol SLC15A4 and Name: solute carrier family 15, member 4 [Homo sapiens]
Other Aliases: FP12591, PHT1, PTR4
Other Designations: peptide-histidine transporter 4
Chromosome: 12; Location: 12q24.32
Annotation: Chromosome 12, NC_000012.10 (127843713..127874494, complement)
GeneID: 121260
190: LCN9  
Official Symbol LCN9 and Name: lipocalin 9 [Homo sapiens]
Other Aliases: 9230102I19Rik
Chromosome: 9; Location: 9q34.3
Annotation: Chromosome 9, NC_000009.10 (137694989..137697770)
GeneID: 392399
191: RBP7  
Official Symbol RBP7 and Name: retinol binding protein 7, cellular [Homo sapiens]
Other Aliases: RP11-496H15.1, CRBP4, CRBPIV, MGC70641
Other Designations: putative cellular retinol-binding protein CRBP IV; retinoid binding protein 7
Chromosome: 1; Location: 1p36.22
Annotation: Chromosome 1, NC_000001.9 (9979861..9998665)
MIM: 608604
GeneID: 116362
192: SLCO1C1  
Official Symbol SLCO1C1 and Name: solute carrier organic anion transporter family, member 1C1 [Homo sapiens]
Other Aliases: OATP-F, OATP1, OATP1C1, SLC21A14
Other Designations: solute carrier family 21 (organic anion transporter), member 14
Chromosome: 12; Location: 12p12.2
Annotation: Chromosome 12, NC_000012.10 (20739666..20797587)
GeneID: 53919
193: OBP2A  
Official Symbol OBP2A and Name: odorant binding protein 2A [Homo sapiens]
Other Aliases: OBP, OBP2C, OBPIIa, hOBPIIa
Other Designations: putative odorant-binding protein 2c
Chromosome: 9; Location: 9q34
Annotation: Chromosome 9, NC_000009.10 (137577806..137581623)
MIM: 164320
GeneID: 29991
194: OBP2B  
Official Symbol OBP2B and Name: odorant binding protein 2B [Homo sapiens]
Other Aliases: MGC119022, hOBPIIb
Other Designations: odorant-binding protein 2B
Chromosome: 9; Location: 9q34
Annotation: Chromosome 9, NC_000009.10 (135070487..135074449, complement)
MIM: 604606
GeneID: 29989
195: SLC39A2  
Official Symbol SLC39A2 and Name: solute carrier family 39 (zinc transporter), member 2 [Homo sapiens]
Other Aliases: MGC119190, ZIP2
Chromosome: 14; Location: 14q11.2
Annotation: Chromosome 14, NC_000014.7 (20537310..20539870)
GeneID: 29986
196: RFC2  
Official Symbol RFC2 and Name: replication factor C (activator 1) 2, 40kDa [Homo sapiens]
Other Aliases: A1, MGC3665, RFC40
Other Designations: replication factor C (activator 1) 2 (40kD); replication factor C 2 (40kD); replication factor C 40 kDa subunit
Chromosome: 7; Location: 7q11.23
Annotation: Chromosome 7, NC_000007.12 (73283768..73306674, complement)
MIM: 600404
GeneID: 5982
197: RBP4  
Official Symbol RBP4 and Name: retinol binding protein 4, plasma [Homo sapiens]
Other Designations: retinol-binding protein 4, interstitial; retinol-binding protein 4, plasma
Chromosome: 10; Location: 10q23-q24
Annotation: Chromosome 10, NC_000010.9 (95341583..95350983, complement)
MIM: 180250
GeneID: 5950
198: RBP2  
Official Symbol RBP2 and Name: retinol binding protein 2, cellular [Homo sapiens]
Other Aliases: CRABP-II, CRBP2, CRBPII, RBPC2
Other Designations: retinol-binding protein 2, cellular
Chromosome: 3; Location: 3q23
Annotation: Chromosome 3, NC_000003.10 (140654416..140678042, complement)
MIM: 180280
GeneID: 5948
199: RBP1  
Official Symbol RBP1 and Name: retinol binding protein 1, cellular [Homo sapiens]
Other Aliases: CRABP-I, CRBP, CRBP1, RBPC
Other Designations: retinol-binding protein 1, cellular
Chromosome: 3; Location: 3q23
Annotation: Chromosome 3, NC_000003.10 (140718970..140741180, complement)
MIM: 180260
GeneID: 5947
200: UNQ2541  
MSFL2541 [Homo sapiens]
Chromosome: 9; Location: 9q34.3
Annotation: Chromosome 9, NC_000009.10 (138773907..138778786, complement)
GeneID: 389812
201: SLC13A5  
Official Symbol SLC13A5 and Name: solute carrier family 13 (sodium-dependent citrate transporter), member 5 [Homo sapiens]
Other Aliases: DKFZp686E17257, MGC138356, NACT
Other Designations: sodium-coupled citrate transporter
Chromosome: 17; Location: 17p13.2
Annotation: Chromosome 17, NC_000017.9 (6528762..6557388, complement)
MIM: 608305
GeneID: 284111
202: SLC35B4  
Official Symbol SLC35B4 and Name: solute carrier family 35, member B4 [Homo sapiens]
Other Aliases: FLJ14697, YEA, YEA4
Other Designations: UDP-Xylose/N-Acetylglucosamine transporter
Chromosome: 7; Location: 7q33
Annotation: Chromosome 7, NC_000007.12 (133624629..133652343, complement)
MIM: 610923
GeneID: 84912
203: SLCO1B1  
Official Symbol SLCO1B1 and Name: solute carrier organic anion transporter family, member 1B1 [Homo sapiens]
Other Aliases: LST-1, MGC133282, OATP-C, OATP1B1, OATP2, SLC21A6
Other Designations: solute carrier family 21 (organic anion transporter), member 6
Chromosome: 12; Location: 12p
Annotation: Chromosome 12, NC_000012.10 (21175403..21283997)
MIM: 604843
GeneID: 10599
204: SLC35A1  
Official Symbol SLC35A1 and Name: solute carrier family 35 (CMP-sialic acid transporter), member A1 [Homo sapiens]
Other Aliases: CMPST, CST, hCST, inactive
Other Designations: CMP-sialic acid transporter; OTTHUMP00000040610; mutated CMP-sialic acid transporter A1; solute carrier family 35 (CMP-sialic acid transporter), member 1; solute carrier family 35 (UDP-galactose transporter), member 1
Chromosome: 6; Location: 6q15
Annotation: Chromosome 6, NC_000006.10 (88239414..88278766)
MIM: 605634
GeneID: 10559
205: PTGDS  
Official Symbol PTGDS and Name: prostaglandin D2 synthase 21kDa (brain) [Homo sapiens]
Other Aliases: PDS, PGD2, PGDS, PGDS2
Other Designations: PGD2 synthase; beta-trace protein; glutathione-independent PGD synthase; lipocalin-type prostaglandin D synthase; prostaglandin D synthase; prostaglandin D2 synthase (21kD, brain); prostaglandin H2 D-isomerase; prostaglandin-H2 D-isomerase
Chromosome: 9; Location: 9q34.2-q34.3
Annotation: Chromosome 9, NC_000009.10 (138991777..138996015)
MIM: 176803
GeneID: 5730
206: CD3D  
Official Symbol CD3D and Name: CD3d molecule, delta (CD3-TCR complex) [Homo sapiens]
Other Aliases: CD3-DELTA, T3D
Other Designations: CD3D antigen, delta polypeptide; CD3d antigen, delta polypeptide (TiT3 complex); T-cell receptor T3 delta chain
Chromosome: 11; Location: 11q23
Annotation: Chromosome 11, NC_000011.8 (117710475..117718533, complement)
MIM: 186790
GeneID: 915
207: MFSD2  
Official Symbol MFSD2 and Name: major facilitator superfamily domain containing 2 [Homo sapiens]
Other Aliases: FLJ14490, FLJ35904, FP1147, HMFN0656, PP10484, RP3-342P20.1
Chromosome: 1; Location: 1p34.2
Annotation: Chromosome 1, NC_000001.9 (40193397..40208215)
GeneID: 84879
208: SLC15A3  
Official Symbol SLC15A3 and Name: solute carrier family 15, member 3 [Homo sapiens]
Other Aliases: FLJ26631, OCTP, PHT2, PTR3, hPTR3
Other Designations: osteoclast transporter hOCTP; peptide transporter 3
Chromosome: 11; Location: 11q12.2
Annotation: Chromosome 11, NC_000011.8 (60461134..60475833, complement)
MIM: 610408
GeneID: 51296
209: FLJ45224
FLJ45224 protein [Homo sapiens]
Other Designations: hypothetical protein LOC401562
Chromosome: 9; Location: 9q34.3
Annotation: Chromosome 9, NC_000009.10 (138996177..139000031)
GeneID: 401562
210: SLC35E1  
Official Symbol SLC35E1 and Name: solute carrier family 35, member E1 [Homo sapiens]
Other Aliases: FLJ14251, MGC44954
Chromosome: 19; Location: 19p13.11
Annotation: Chromosome 19, NC_000019.8 (16523564..16544193, complement)
GeneID: 79939
211: SLC39A1  
Official Symbol SLC39A1 and Name: solute carrier family 39 (zinc transporter), member 1 [Homo sapiens]
Other Aliases: ZIP1, ZIRTL
Other Designations: solute carrier family 39 (zinc transporter), member 3; zinc-iron regulated transporter-like; zinc/iron regulated transporter-like
Chromosome: 1; Location: 1q21
Annotation: Chromosome 1, NC_000001.9 (152198212..152206812, complement)
MIM: 604740
GeneID: 27173
212: C8G  
Official Symbol C8G and Name: complement component 8, gamma polypeptide [Homo sapiens]
Other Aliases: C8C, MGC142186
Chromosome: 9; Location: 9q34.3
Annotation: Chromosome 9, NC_000009.10 (138959534..138961240)
MIM: 120930
GeneID: 733
213: LCN12  
Official Symbol LCN12 and Name: lipocalcin 12 [Homo sapiens]
Other Aliases: RP11-229P13.4, MGC34753, MGC48935
Other Designations: OTTHUMP00000022666; OTTHUMP00000022670; lipocalin 12
Chromosome: 9; Location: 9q34.3
Annotation: Chromosome 9, NC_000009.10 (138966589..138969770)
GeneID: 286256
214: SLC35B3  
Official Symbol SLC35B3 and Name: solute carrier family 35, member B3 [Homo sapiens]
Other Aliases: C6orf196, CGI-19, PAPST2
Other Designations: 3' phosphoadenosine 5' phosphosulfate transporter 2; 3'-phosphoadenosine 5'-phosphosulfate transporter; OTTHUMP00000039206
Chromosome: 6; Location: 6p24.3
Annotation: Chromosome 6, NC_000006.10 (8358306..8380624, complement)
MIM: 610845
GeneID: 51000
215: PMP2  
Official Symbol PMP2 and Name: peripheral myelin protein 2 [Homo sapiens]
Other Aliases: FABP8, M-FABP, MP2, P2
Chromosome: 8; Location: 8q21.3-q22.1
Annotation: Chromosome 8, NC_000008.9 (82515116..82522274, complement)
MIM: 170715
GeneID: 5375
216: LST-3TM12
organic anion transporter LST-3b [Homo sapiens]
Other Aliases: LST3
Other Designations: liver-specific organic anion transporter 3; liver-specific organic anion transporter 3TM12
Chromosome: 12; Location: 12p12.2
Annotation: Chromosome 12, NC_000012.10 (20859874..21134446)
GeneID: 338821
217: SLCO4C1  
Official Symbol SLCO4C1 and Name: solute carrier organic anion transporter family, member 4C1 [Homo sapiens]
Other Aliases: OATP-H, OATP-M1, OATP4C1, OATPX, PRO2176, SLC21A20
Chromosome: 5; Location: 5q21.2
Annotation: Chromosome 5, NC_000005.8 (101597589..101660152, complement)
MIM: 609013
GeneID: 353189
218: SLC35E3  
Official Symbol SLC35E3 and Name: solute carrier family 35, member E3 [Homo sapiens]
Other Aliases: BLOV1
Other Designations: bladder cancer overexpressed protein; solute carrier family 35, member E2
Chromosome: 12; Location: 12q15
Annotation: Chromosome 12, NC_000012.10 (67426203..67446120)
GeneID: 55508
219: APOD  
Official Symbol APOD and Name: apolipoprotein D [Homo sapiens]
Chromosome: 3; Location: 3q26.2-qter
Annotation: Chromosome 3, NC_000003.10 (196776865..196792278, complement)
MIM: 107740
GeneID: 347
220: SLC9A4
Official Symbol SLC9A4 and Name: solute carrier family 9 (sodium/hydrogen exchanger), member 4 [Homo sapiens]
Other Aliases: DKFZp313B031, NHE4
Other Designations: solute carrier family 9 (sodium/hydrogen exchanger), isoform 4
Chromosome: 2; Location: 2q12.1
Annotation: Chromosome 2, NC_000002.10 (102456194..102516859)
MIM: 600531
GeneID: 389015
221: SLC39A12  
Official Symbol SLC39A12 and Name: solute carrier family 39 (zinc transporter), member 12 [Homo sapiens]
Other Aliases: FLJ30499, MGC43205, MGC51099, bA570F3.1
Other Designations: solute carrier family 39 (metal ion transporter), member 12
Chromosome: 10; Location: 10p12.33
Annotation: Chromosome 10, NC_000010.9 (18280827..18372218)
GeneID: 221074
222: SLC26A10
Official Symbol SLC26A10 and Name: solute carrier family 26, member 10 [Homo sapiens]
Chromosome: 12; Location: 12q13
Annotation: Chromosome 12, NC_000012.10 (56299960..56306201)
GeneID: 65012
223: ORM2  
Official Symbol ORM2 and Name: orosomucoid 2 [Homo sapiens]
Other Aliases: AGP-B, AGP-B', AGP2
Other Designations: alpha-1-acid glycoprotein, type 2
Chromosome: 9; Location: 9q32
Annotation: Chromosome 9, NC_000009.10 (116131890..116135357)
MIM: 138610
GeneID: 5005
224: ORM1  
Official Symbol ORM1 and Name: orosomucoid 1 [Homo sapiens]
Other Aliases: AGP-A, AGP1, ORM
Other Designations: Orosomucoid-1 (alpha-1-acid glycoprotein-1); alpha-1-acid glycoprotein 1
Chromosome: 9; Location: 9q31-q32
Annotation: Chromosome 9, NC_000009.10 (116125157..116128578)
MIM: 138600
GeneID: 5004
225: AMBP  
Official Symbol AMBP and Name: alpha-1-microglobulin/bikunin precursor [Homo sapiens]
Other Aliases: HCP, ITI, ITIL, UTI
Other Designations: Alpha-1-microglobulin/bikunin precursor (inter-alpha-trypsin inhibitor, light chain; protein HC); Alpha-1-microglobulin/bikunin precursor; inter-alpha-trypsin; OTTHUMP00000063975; alpha-1-microglobulin/bikunin; growth-inhibiting protein 19
Chromosome: 9; Location: 9q32-q33
Annotation: Chromosome 9, NC_000009.10 (115862228..115880536, complement)
MIM: 176870
GeneID: 259
226: SLC36A4  
Official Symbol SLC36A4 and Name: solute carrier family 36 (proton/amino acid symporter), member 4 [Homo sapiens]
Other Aliases: FLJ38932, PAT4
Other Designations: proton/amino acid transporter 4
Chromosome: 11; Location: 11q21
Annotation: Chromosome 11, NC_000011.8 (92520498..92570743, complement)
GeneID: 120103
227: SLCO5A1  
Official Symbol SLCO5A1 and Name: solute carrier organic anion transporter family, member 5A1 [Homo sapiens]
Other Aliases: FLJ39560, OATP-J, OATP5A1, OATPRP4, SLC21A15
Other Designations: organic anion transporter polypeptide-related protein 4; solute carrier family 21 (organic anion transporter), member 15
Chromosome: 8; Location: 8q13.3
Annotation: Chromosome 8, NC_000008.9 (70747129..70909762, complement)
GeneID: 81796
228: SLC7A14  
Official Symbol SLC7A14 and Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 14 [Homo sapiens]
Other Aliases: KIAA1613
Chromosome: 3; Location: 3q26.2
Annotation: Chromosome 3, NC_000003.10 (171667255..171786552, complement)
GeneID: 57709
229: SLC35C1  
Official Symbol SLC35C1 and Name: solute carrier family 35, member C1 [Homo sapiens]
Other Aliases: FLJ11320, FLJ14841, FUCT1
Other Designations: GDP-fucose transporter 1
Chromosome: 11; Location: 11p11.2
Annotation: Chromosome 11, NC_000011.8 (45783912..45791143)
MIM: 605881
GeneID: 55343
230: SLC39A9  
Official Symbol SLC39A9 and Name: solute carrier family 39 (zinc transporter), member 9 [Homo sapiens]
Other Aliases: FLJ11274, MGC74989
Other Designations: solute carrier family 39 member 9; zinc transporter
Chromosome: 14; Location: 14q24.1
Annotation: Chromosome 14, NC_000014.7 (68935704..68997021)
GeneID: 55334
231: TMEM144  
Official Symbol TMEM144 and Name: transmembrane protein 144 [Homo sapiens]
Other Aliases: FLJ11155
Other Designations: hypothetical protein LOC55314
Chromosome: 4; Location: 4q32.1
Annotation: Chromosome 4, NC_000004.10 (159351126..159395889)
GeneID: 55314
232: SLC36A3  
Official Symbol SLC36A3 and Name: solute carrier family 36 (proton/amino acid symporter), member 3 [Homo sapiens]
Other Aliases: FLJ16658, MGC119638, MGC119639, MGC119641, PAT3, TRAMD2, tramdorin2
Other Designations: proton/amino acid transporter 3; tramdorin 2
Chromosome: 5; Location: 5q33.1
Annotation: Chromosome 5, NC_000005.8 (150636516..150663520, complement)
MIM: 608332
GeneID: 285641
233: FLJ39822  
hypothetical protein FLJ39822 [Homo sapiens]
Other Aliases: MGC150450
Other Designations: hypothetical protein LOC151258
Chromosome: 2; Location: 2q24.3
Annotation: Chromosome 2, NC_000002.10 (165463058..165520281, complement)
GeneID: 151258
234: TMEM163  
Official Symbol TMEM163 and Name: transmembrane protein 163 [Homo sapiens]
Other Aliases: DC29, DKFZP566N034, DKFZp666J217
Other Designations: hypothetical protein LOC81615
Chromosome: 2; Location: 2q21.3
Annotation: Chromosome 2, NC_000002.10 (134930030..135193040, complement)
GeneID: 81615
235: FLJ10815  
amino acid transporter [Homo sapiens]
Other Aliases: FLJ12724
Chromosome: 16; Location: 16q21
Annotation: Chromosome 16, NC_000016.8 (57257799..57276175, complement)
GeneID: 55238
236: TAAR6  
Official Symbol TAAR6 and Name: trace amine associated receptor 6 [Homo sapiens]
Other Aliases: RP11-295F4.3, SCZD5, TA4, TRAR4
Other Designations: trace amine receptor 4
Chromosome: 6; Location: 6q23.2
Annotation: Chromosome 6, NC_000006.10 (132933154..132934191)
MIM: 608923
GeneID: 319100
237: TPMT  
Official Symbol TPMT and Name: thiopurine S-methyltransferase [Homo sapiens]
Other Designations: S-adenosyl-L-methionine:thiopurine S-methyltransferase; thiopurine methyltransferase
Chromosome: 6; Location: 6p22.3
Annotation: Chromosome 6, NC_000006.10 (18236521..18263353, complement)
MIM: 187680
GeneID: 7172
238: PICK1  
Official Symbol PICK1 and Name: protein interacting with PRKCA 1 [Homo sapiens]
Other Aliases: MGC15204, PRKCABP
Other Designations: OTTHUMP00000028509; PRKCA-binding protein; protein interacting with C kinase 1; protein kinase C, alpha binding protein
Chromosome: 22; Location: 22q13.1
Annotation: Chromosome 22, NC_000022.9 (36783208..36801654)
MIM: 605926
GeneID: 9463
239: TK2
Official Symbol TK2 and Name: thymidine kinase 2, mitochondrial [Homo sapiens]
Chromosome: 16; Location: 16q22-q23.1
Annotation: Chromosome 16, NC_000016.8 (65100846..65141816, complement)
MIM: 188250
GeneID: 7084
240: MYO5B
Official Symbol MYO5B and Name: myosin VB [Homo sapiens]
Other Aliases: KIAA1119
Chromosome: 18; Location: 18q21
Annotation: Chromosome 18, NC_000018.8 (45603099..45975382, complement)
MIM: 606540
GeneID: 4645
241: MUC4
Official Symbol MUC4 and Name: mucin 4, cell surface associated [Homo sapiens]
Other Aliases: HSA276359
Other Designations: mucin 4; mucin 4, tracheobronchial
Chromosome: 3; Location: 3q29
Annotation: Chromosome 3, NC_000003.10 (196959307..197023545, complement)
MIM: 158372
GeneID: 4585
242: ESR1  
Official Symbol ESR1 and Name: estrogen receptor 1 [Homo sapiens]
Other Aliases: RP1-130E4.1, DKFZp686N23123, ER, ESR, ESRA, Era, NR3A1
Other Designations: dJ443C4.1.1 (estrogen receptor 1); estrogen receptor 1 (alpha); oestrogen receptor; steroid hormone receptor
Chromosome: 6; Location: 6q25.1
Annotation: Chromosome 6, NC_000006.10 (152170379..152466099)
MIM: 133430
GeneID: 2099
243: RHBG  
Official Symbol RHBG and Name: Rh family, B glycoprotein [Homo sapiens]
Other Designations: Rh type B glycoprotein; Rhesus blood group, B glycoprotein
Chromosome: 1; Location: 1q21.3
Annotation: Chromosome 1, NC_000001.9 (154605627..154621635)
MIM: 607079
GeneID: 57127
244: SLC39A14  
Official Symbol SLC39A14 and Name: solute carrier family 39 (zinc transporter), member 14 [Homo sapiens]
Other Aliases: KIAA0062, LZT-Hs4, ZIP14, cig19
Other Designations: Zrt-, Irt-like protein 14; solute carrier family 39 (metal ion transporter), member 14
Chromosome: 8; Location: 8p21.3
Annotation: Chromosome 8, NC_000008.9 (22280737..22336143)
MIM: 608736
GeneID: 23516
245: SLC28A2  
Official Symbol SLC28A2 and Name: solute carrier family 28 (sodium-coupled nucleoside transporter), member 2 [Homo sapiens]
Other Aliases: CNT2, HCNT2, HsT17153, MGC138252, SPNT1
Chromosome: 15; Location: 15q15
Annotation: Chromosome 15, NC_000015.8 (43331726..43355425)
MIM: 606208
GeneID: 9153
246: SNCA  
Official Symbol SNCA and Name: synuclein, alpha (non A4 component of amyloid precursor) [Homo sapiens]
Other Aliases: MGC110988, NACP, PARK1, PARK4, PD1
Other Designations: alpha synuclein; alpha-synuclein; alpha-synuclein, isoform NACP140; non A-beta component of AD amyloid; non A4 component of amyloid
Chromosome: 4; Location: 4q21
Annotation: Chromosome 4, NC_000004.10 (90865728..90977156, complement)
MIM: 163890
GeneID: 6622
247: TOR1A  
Official Symbol TOR1A and Name: torsin family 1, member A (torsin A) [Homo sapiens]
Other Aliases: DQ2, DYT1, torsin A
Other Designations: dystonia 1, torsion (autosomal dominant; torsin A); torsin A
Chromosome: 9; Location: 9q34
Annotation: Chromosome 9, NC_000009.10 (131615042..131626262, complement)
MIM: 605204
GeneID: 1861
248: DRD3  
Official Symbol DRD3 and Name: dopamine receptor D3 [Homo sapiens]
Other Aliases: D3DR, ETM1, FET1, MGC149204, MGC149205
Other Designations: essential tremor 1
Chromosome: 3; Location: 3q13.3
Annotation: Chromosome 3, NC_000003.10 (115330247..115380589, complement)
MIM: 126451
GeneID: 1814
249: DRD2  
Official Symbol DRD2 and Name: dopamine receptor D2 [Homo sapiens]
Other Aliases: D2DR, D2R
Other Designations: seven transmembrane helix receptor
Chromosome: 11; Location: 11q23
Annotation: Chromosome 11, NC_000011.8 (112785527..112851091, complement)
MIM: 126450
GeneID: 1813
250: DRD1  
Official Symbol DRD1 and Name: dopamine receptor D1 [Homo sapiens]
Other Aliases: DADR, DRD1A
Chromosome: 5; Location: 5q35.1
Annotation: Chromosome 5, NC_000005.8 (174800281..174803769, complement)
MIM: 126449
GeneID: 1812
251: DPYD  
Official Symbol DPYD and Name: dihydropyrimidine dehydrogenase [Homo sapiens]
Other Aliases: DHP, DPD, MGC132008, MGC70799
Other Designations: OTTHUMP00000058954
Chromosome: 1; Location: 1p22
Annotation: Chromosome 1, NC_000001.9 (97315890..98159167, complement)
MIM: 274270
GeneID: 1806
252: SLC22A9  
Official Symbol SLC22A9 and Name: solute carrier family 22 (organic anion/cation transporter), member 9 [Homo sapiens]
Other Aliases: FLJ23666, HOAT4, OAT4, OAT7, UST3H, ust3
Other Designations: organic anion transporter 4; organic anion transporter 7
Chromosome: 11; Location: 11q13.1
Annotation: Chromosome 11, NC_000011.8 (62893837..62934307)
MIM: 607579
GeneID: 114571
253: SLC22A5  
Official Symbol SLC22A5 and Name: solute carrier family 22 (organic cation transporter), member 5 [Homo sapiens]
Other Aliases: CDSP, FLJ46769, OCTN2, OCTN2VT
Other Designations: high-affinity sodium dependent carnitine cotransporter; organic cation transporter 2; organic cation transporter 5; organic cation/carnitine transporter 2; solute carrier family 22 member 5
Chromosome: 5; Location: 5q31
Annotation: Chromosome 5, NC_000005.8 (131733343..131759205)
MIM: 603377
GeneID: 6584
254: SLC22A4  
Official Symbol SLC22A4 and Name: solute carrier family 22 (organic cation transporter), member 4 [Homo sapiens]
Other Aliases: MGC34546, MGC40524, OCTN1
Other Designations: integral membrane transport protein; organic cation transporter 4; solute carrier family 22 member 4
Chromosome: 5; Location: 5q31.1
Annotation: Chromosome 5, NC_000005.8 (131658044..131707798)
MIM: 604190
GeneID: 6583
255: SLC22A3
Official Symbol SLC22A3 and Name: solute carrier family 22 (extraneuronal monoamine transporter), member 3 [Homo sapiens]
Other Aliases: EMT, EMTH, OCT3
Other Designations: EMT organic cation transporter 3; extraneuronal monoamine transporter; organic cation transporter 3; solute carrier family 22 member 3
Chromosome: 6; Location: 6q26-q27
Annotation: Chromosome 6, NC_000006.10 (160689415..160796004)
MIM: 604842
GeneID: 6581
256: SLC34A1  
Official Symbol SLC34A1 and Name: solute carrier family 34 (sodium phosphate), member 1 [Homo sapiens]
Other Aliases: NAPI-3, NPT2, NPTIIa, SLC11, SLC17A2
Other Designations: Na+-phosphate cotransporter type II; sodium/phosphate co-transporter; solute carrier family 17 (sodium phosphate), member 2
Chromosome: 5; Location: 5q35
Annotation: Chromosome 5, NC_000005.8 (176744061..176758455)
MIM: 182309
GeneID: 6569
257: SLC7A2  
Official Symbol SLC7A2 and Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 2 [Homo sapiens]
Other Aliases: ATRC2, CAT-2, HCAT2
Other Designations: amino acid transporter, cationic 2; cationic amino acid transporter, y+ system; low-affinity cationic amino acid transporter-2; solute carrier family 7, member 2
Chromosome: 8; Location: 8p22-p21.3
Annotation: Chromosome 8, NC_000008.9 (17440685..17472300)
MIM: 601872
GeneID: 6542
258: SLC7A1  
Official Symbol SLC7A1 and Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 1 [Homo sapiens]
Other Aliases: RP11-274A8.1, ATRC1, CAT-1, ERR, HCAT1, REC1L
Other Designations: OTTHUMP00000042418; amino acid transporter, cationic 1; ecotropic retroviral receptor
Chromosome: 13; Location: 13q12-q14
Annotation: Chromosome 13, NC_000013.9 (28981551..29067721, complement)
MIM: 104615
GeneID: 6541
259: SLC6A11
Official Symbol SLC6A11 and Name: solute carrier family 6 (neurotransmitter transporter, GABA), member 11 [Homo sapiens]
Other Aliases: GAT-3, GAT3
Chromosome: 3; Location: 3p25.3
Annotation: Chromosome 3, NC_000003.10 (10832917..10955146)
MIM: 607952
GeneID: 6538
260: SLC6A2
Official Symbol SLC6A2 and Name: solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 [Homo sapiens]
Other Aliases: NAT1, NET, NET1, SLC6A5
Other Designations: noradrenaline transporter; norepinephrine transporter; solute carrier family 6 (neurotransmitter transporter, norepinephrine), member 5; solute carrier family 6 member 2
Chromosome: 16; Location: 16q12.2
Annotation: Chromosome 16, NC_000016.8 (54248057..54295201)
MIM: 163970
GeneID: 6530
261: SLC5A1  
Official Symbol SLC5A1 and Name: solute carrier family 5 (sodium/glucose cotransporter), member 1 [Homo sapiens]
Other Aliases: RP1-127L4.1, D22S675, NAGT, SGLT1
Other Designations: Human Na+/glucose cotransporter 1 mRNA, complete cds; solute carrier family 5 (sodium/glucose transporter), member 1
Chromosome: 22; Location: 22q12.3
Annotation: Chromosome 22, NC_000022.9 (30769259..30836645)
MIM: 182380
GeneID: 6523
262: SLC3A2  
Official Symbol SLC3A2 and Name: solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2 [Homo sapiens]
Other Aliases: 4F2, 4F2HC, 4T2HC, CD98, CD98HC, MDU1, NACAE
Other Designations: 4F2 cell-surface antigen heavy chain; 4F2 heavy chain; CD98 heavy chain; antigen defined by monoclonal antibody 4F2, heavy chain; antigen identified by monoclonal antibodies 4F2, TRA1.10, TROP4, and T43; lymphocyte activation antigen 4F2 large subunit; monoclonal antibody 44D7
Chromosome: 11; Location: 11q13
Annotation: Chromosome 11, NC_000011.8 (62380094..62412929)
MIM: 158070
GeneID: 6520
263: SLC28A3  
Official Symbol SLC28A3 and Name: solute carrier family 28 (sodium-coupled nucleoside transporter), member 3 [Homo sapiens]
Other Aliases: CNT3
Other Designations: concentrative Na+-nucleoside cotransporter
Chromosome: 9; Location: 9q22.2
Annotation: Chromosome 9, NC_000009.10 (86082912..86173233, complement)
MIM: 608269
GeneID: 64078
264: TIMM8A  
Official Symbol TIMM8A and Name: translocase of inner mitochondrial membrane 8 homolog A (yeast) [Homo sapiens]
Other Aliases: DDP, DDP1, DFN1, MGC12262, MTS
Other Designations: deafness/dystonia peptide; translocase of inner mitochondrial membrane 8 homolog A
Chromosome: X; Location: Xq22.1
Annotation: Chromosome X, NC_000023.9 (100487306..100490343, complement)
MIM: 300356
GeneID: 1678
265: SLC19A3  
Official Symbol SLC19A3 and Name: solute carrier family 19, member 3 [Homo sapiens]
Chromosome: 2; Location: 2q37
Annotation: Chromosome 2, NC_000002.10 (228258170..228290989, complement)
MIM: 606152
GeneID: 80704
266: RAB11A  
Official Symbol RAB11A and Name: RAB11A, member RAS oncogene family [Homo sapiens]
Other Aliases: MGC1490, YL8
Other Designations: RAB 11A, member oncogene family; Ras-related protein Rab-11A
Chromosome: 15; Location: 15q21.3-q22.31
Annotation: Chromosome 15, NC_000015.8 (63948850..63968846)
MIM: 605570
GeneID: 8766
267: SLC43A1  
Official Symbol SLC43A1 and Name: solute carrier family 43, member 1 [Homo sapiens]
Other Aliases: LAT3, PB39, POV1, R00504
Other Designations: L-type amino acid transporter 3; prostate cancer overexpressed gene 1
Chromosome: 11; Location: 11p11.2-p11.1
Annotation: Chromosome 11, NC_000011.8 (57008583..57039735, complement)
MIM: 603733
GeneID: 8501
268: ABCC13
Official Symbol ABCC13 and Name: ATP-binding cassette, sub-family C (CFTR/MRP), member 13 [Homo sapiens]
Other Aliases: C21orf73, PRED6
Other Designations: ATP-binding cassette protein C13
Chromosome: 21; Location: 21q11.2
Annotation: Chromosome 21, NC_000021.7 (14567991..14595600)
MIM: 608835
GeneID: 150000
269: SLC22A7  
Official Symbol SLC22A7 and Name: solute carrier family 22 (organic anion transporter), member 7 [Homo sapiens]
Other Aliases: MGC24091, MGC45202, NLT, OAT2
Other Designations: liver-specific transporter; organic anion transporter 2; solute carrier family 22 member 7
Chromosome: 6; Location: 6p21.2-p21.1
Annotation: Chromosome 6, NC_000006.10 (43373976..43381254)
MIM: 604995
GeneID: 10864
270: ABCE1  
Official Symbol ABCE1 and Name: ATP-binding cassette, sub-family E (OABP), member 1 [Homo sapiens]
Other Aliases: ABC38, OABP, RLI, RNASEL1, RNASELI, RNS4I
Other Designations: ATP-binding cassette, sub-family E, member 1; RNase L inhibitor; ribonuclease L (2',5'-oligoisoadenylate synthetase-dependent) inhibitor
Chromosome: 4; Location: 4q31
Annotation: Chromosome 4, NC_000004.10 (146238931..146269781)
MIM: 601213
GeneID: 6059
271: CLCN5  
Official Symbol CLCN5 and Name: chloride channel 5 (nephrolithiasis 2, X-linked, Dent disease) [Homo sapiens]
Other Aliases: CLC5, CLCK2, DENTS, NPHL2, XLRH, XRN, hCIC-K2, hClC-K2
Other Designations: chloride channel 5
Chromosome: X; Location: Xp11.23-p11.22
Annotation: Chromosome X, NC_000023.9 (49720896..49744261)
MIM: 300008
GeneID: 1184
272: SLC7A3  
Official Symbol SLC7A3 and Name: solute carrier family 7 (cationic amino acid transporter, y+ system), member 3 [Homo sapiens]
Other Aliases: ATRC3, CAT-3, FLJ14541, MGC20687
Chromosome: X; Location: Xq13.1
Annotation: Chromosome X, NC_000023.9 (70062154..70067655, complement)
MIM: 300443
GeneID: 84889
273: MAPK1  
Official Symbol MAPK1 and Name: mitogen-activated protein kinase 1 [Homo sapiens]
Other Aliases: ERK, ERK2, ERT1, MAPK2, P42MAPK, PRKM1, PRKM2, p38, p40, p41, p41mapk
Other Designations: extracellular signal-regulated kinase 2; mitogen-activated protein kinase 2; protein tyrosine kinase ERK2
Chromosome: 22; Location: 22q11.21
Annotation: Chromosome 22, NC_000022.9 (20443946..20551970, complement)
MIM: 176948
GeneID: 5594
274: SLC22A11  
Official Symbol SLC22A11 and Name: solute carrier family 22 (organic anion/cation transporter), member 11 [Homo sapiens]
Other Aliases: MGC34282, OAT4, hOAT4
Other Designations: organic anion transporter 4; solute carrier family 22 member 11
Chromosome: 11; Location: 11q13.1
Annotation: Chromosome 11, NC_000011.8 (64079674..64095575)
MIM: 607097
GeneID: 55867
275: GRM5
Official Symbol GRM5 and Name: glutamate receptor, metabotropic 5 [Homo sapiens]
Other Aliases: GPRC1E, MGLUR5, MGLUR5A, MGLUR5B, mGlu5
Chromosome: 11; Location: 11q14.2-q14.3
Annotation: Chromosome 11, NC_000011.8 (87880626..88420838, complement)
MIM: 604102
GeneID: 2915
276: GRM3  
Official Symbol GRM3 and Name: glutamate receptor, metabotropic 3 [Homo sapiens]
Other Aliases: GLUR3, GPRC1C, MGLUR3, mGlu3
Chromosome: 7; Location: 7q21.1-q21.2
Annotation: Chromosome 7, NC_000007.12 (86111166..86332128)
MIM: 601115
GeneID: 2913
277: ATP7B  
Official Symbol ATP7B and Name: ATPase, Cu++ transporting, beta polypeptide [Homo sapiens]
Other Aliases: RP11-327P2.3, PWD, WC1, WD, WND
Other Designations: ATPase, Cu(2+)- transporting, beta polypeptide; OTTHUMP00000040880; Wilson disease; Wilson disease-associated protein; copper pump 2; copper-transporting ATPase 2
Chromosome: 13; Location: 13q14.3
Annotation: Chromosome 13, NC_000013.9 (51404806..51483631, complement)
MIM: 606882
GeneID: 540
278: SLC47A2  
Official Symbol SLC47A2 and Name: solute carrier family 47, member 2 [Homo sapiens]
Other Aliases: FLJ31196, MATE2, MATE2-B, MATE2-K
Other Designations: H+/organic cation antiporter; multidrug and toxin extrusion 2
Chromosome: 17; Location: 17p11.2
Annotation: Chromosome 17, NC_000017.9 (19522220..19560515, complement)
MIM: 609833
GeneID: 146802
279: ATP2B4
Official Symbol ATP2B4 and Name: ATPase, Ca++ transporting, plasma membrane 4 [Homo sapiens]
Other Aliases: ATP2B2, DKFZp686G08106, DKFZp686M088, MXRA1, PMCA4, PMCA4b, PMCA4x
Other Designations: matrix-remodelling associated 1; plasma membrane calcium ATPase 4; plasma membrane calcium pump; sarcolemmal calcium pump
Chromosome: 1; Location: 1q32.1
Annotation: Chromosome 1, NC_000001.9 (201862551..201979832)
MIM: 108732
GeneID: 493
280: ATP1A1  
Official Symbol ATP1A1 and Name: ATPase, Na+/K+ transporting, alpha 1 polypeptide [Homo sapiens]
Other Aliases: MGC3285, MGC51750
Other Designations: G00-119-711; Na+, K+ ATPase alpha subunit; Na+/K+ -ATPase alpha 1 subunit; Na+/K+ ATPase 1; Na, K-ATPase, alpha-A catalytic polypeptide; Na,K-ATPase alpha-1 subunit; Na,K-ATPase catalytic subunit alpha-A protein; Na/K-ATPase alpha subunit fragment (aa 1-149); sodium pump 1; sodium-potassium-ATPase, alpha 1 polypeptide
Chromosome: 1; Location: 1p21
Annotation: Chromosome 1, NC_000001.9 (116717359..116748919)
MIM: 182310
GeneID: 476
281: PARK2  
Official Symbol PARK2 and Name: Parkinson disease (autosomal recessive, juvenile) 2, parkin [Homo sapiens]
Other Aliases: AR-JP, LPRS2, PDJ, PRKN
Other Designations: E3 ubiquitin ligase; parkin; parkin 2
Chromosome: 6; Location: 6q25.2-q27
Annotation: Chromosome 6, NC_000006.10 (161689661..163068793, complement)
MIM: 602544
GeneID: 5071
282: TIMM13  
Official Symbol TIMM13 and Name: translocase of inner mitochondrial membrane 13 homolog (yeast) [Homo sapiens]
Other Aliases: TIM13, TIM13B, TIMM13A, TIMM13B, ppv1
Other Designations: mitochondrial import inner membrane translocase subunit Tim13B; translocase of inner mitochondrial membrane 13
Chromosome: 19; Location: 19p13.3
Annotation: Chromosome 19, NC_000019.8 (2376622..2378875, complement)
MIM: 607383
GeneID: 26517
283: ADK  
Official Symbol ADK and Name: adenosine kinase [Homo sapiens]
Other Aliases: AK
Other Designations: adenosine 5'-phosphotransferase
Chromosome: 10; Location: 10q11-q24
Annotation: Chromosome 10, NC_000010.9 (75580971..76139066)
MIM: 102750
GeneID: 132
284: SLC13A3  
Official Symbol SLC13A3 and Name: solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 3 [Homo sapiens]
Other Aliases: RP1-257E24.1, NADC3, SDCT2
Other Designations: Na(+)/dicarboxylate cotransporter 3; sodium-dependent high affinity dicarboxylate transporter 3; solute carrier family 13 member 3
Chromosome: 20; Location: 20q12-q13.1
Annotation: Chromosome 20, NC_000020.9 (44619870..44746514, complement)
MIM: 606411
GeneID: 64849
285: SLC10A6  
Official Symbol SLC10A6 and Name: solute carrier family 10 (sodium/bile acid cotransporter family), member 6 [Homo sapiens]
Other Aliases: MGC129575, MGC129576, SOAT
Other Designations: sodium-dependent organic anion transporter
Chromosome: 4; Location: 4q21.3
Annotation: Chromosome 4, NC_000004.10 (87963865..87989292, complement)
GeneID: 345274
286: SLC10A2  
Official Symbol SLC10A2 and Name: solute carrier family 10 (sodium/bile acid cotransporter family), member 2 [Homo sapiens]
Other Aliases: ASBT, ISBT, NTCP2
Other Designations: OTTHUMP00000040691; ileal apical sodium-dependent bile acid transporter; ileal sodium-dependent bile acid transporter
Chromosome: 13; Location: 13q33
Annotation: Chromosome 13, NC_000013.9 (102494351..102517197, complement)
MIM: 601295
GeneID: 6555
287: SLC10A3  
Official Symbol SLC10A3 and Name: solute carrier family 10 (sodium/bile acid cotransporter family), member 3 [Homo sapiens]
Other Aliases: XX-FW89031B12.2, DXS253E, P3
Other Designations: OTTHUMP00000061456; Protein P3; solute carrier family 10, member 3
Chromosome: X; Location: Xq28
Annotation: Chromosome X, NC_000023.9 (153368842..153372189, complement)
MIM: 312090
GeneID: 8273