| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 25: | LOC652058 | |
| similar to solute carrier
family 29 (nucleoside transporters), member 4 [Homo sapiens] Chromosome: Un GeneID: 652058 |
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| 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 |
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| 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 |
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| 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 |
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| 29: | LOC654078 | |
| similar to solute carrier
family 29 (nucleoside transporters), member 4 [Homo sapiens] Chromosome: 7 GeneID: 654078 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 76: | LOC388931 | |
| hypothetical protein LOC388931
[Homo sapiens] Chromosome: 2; Location: 2p23.3 Annotation: Chromosome 2, NC_000002.10 (24086457..24100649) GeneID: 388931 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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| 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 |
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