| 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 |