Transporters in the liver:
1: TAP1 transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) [Homo sapiens]Other Aliases: HGNC:43, ABC17, ABCB2, APT1, D6S114E, PSF1, RING4Other Designations: ABC transporter, MHC 1; 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, ATP-binding cassette, major histocompatibility complex, 1Chromosome: 6; Location: 6p21.3GeneID: 6890 2: SLC22A3 solute carrier family 22 (extraneuronal monoamine transporter), member 3 [Homo sapiens]Other Aliases: HGNC:10967, EMT, EMTH, OCT3Other Designations: EMT organic cation transporter 3; extraneuronal monoamine transporter; organic cation transporter 3; solute carrier family 22 member 3Chromosome: 6; Location: 6q26-q27GeneID: 6581 3: SLC22A5 solute carrier family 22 (organic cation transporter), member 5 [Homo sapiens]Other Aliases: HGNC:10969, OCTN2Other Designations: high-affinity sodium dependent carnitine cotransporter; organic cation transporter 5; organic cation/carnitine transporter 2; solute carrier family 22 member 5Chromosome: 5; Location: 5q31GeneID: 6584 4: SLCO1A2 solute carrier organic anion transporter family, member 1A2 [Homo sapiens]Other Aliases: HGNC:10956, OATP, OATP-A, OATP1A2, SLC21A3Other Designations: organic anion transporting polypeptide A; sodium-independent organic anion transporter; solute carrier family 21 (organic anion transporter), member 3Chromosome: 12; Location: 12p12GeneID: 6579 5: SLC26A1 solute carrier family 26 (sulfate transporter), member 1 [Homo sapiens]Other Aliases: HGNC:10993, EDM4, SAT-1, SAT1Other Designations: solute carrier family 26, member 1; sulfate anion tranporter AT1; sulfate transporter; sulfate/anion transporter SAT-1 proteinChromosome: 4; Location: 4p16.3GeneID: 10861 6: SLC22A2 solute carrier family 22 (organic cation transporter), member 2 [Homo sapiens]Other Aliases: HGNC:10966, OCT2Other Designations: organic cation transporter 2; solute carrier family 22 member 2Chromosome: 6; Location: 6q26GeneID: 6582 7: SLC22A1 solute carrier family 22 (organic cation transporter), member 1 [Homo sapiens]Other Aliases: HGNC:10963, HOCT1, OCT1Other Designations: organic cation transporter 1; solute carrier family 22 member 1Chromosome: 6; Location: 6q26GeneID: 6580 8: SLC13A5 solute carrier family 13 (sodium-dependent citrate transporter), member 5 [Homo sapiens]Other Aliases: HGNC:23089, NACTOther Designations: sodium-coupled citrate transporterChromosome: 17; Location: 17p13.1GeneID: 284111 9: FABP1 fatty acid binding protein 1, liver [Homo sapiens]Other Aliases: HGNC:3555, FABPL, L-FABPOther Designations: Fatty acid-binding protein, liverChromosome: 2; Location: 2p11GeneID: 2168 10: SLC22A4 solute carrier family 22 (organic cation transporter), member 4 [Homo sapiens]Other Aliases: HGNC:10968, MGC34546, OCTN1Other Designations: integral membrane transport protein; organic cation transporter 4; solute carrier family 22 member 4Chromosome: 5; Location: 5q23.3GeneID: 6583 11: CDH17 cadherin 17, LI cadherin (liver-intestine) [Homo sapiens]Other Aliases: HGNC:1756, CDH16, HPT-1, HPT1Other Designations: HPT-1 cadherin; LI cadherin; cadherin 17; cadherin-16; human intestinal peptide-associated transporter HPT-1; human peptide transporter 1; liver-intestine cadherinChromosome: 8; Location: 8q22.1GeneID: 1015 12: SLC38A4 solute carrier family 38, member 4 [Homo sapiens]Other Aliases: HGNC:14679, ATA3, FLJ10191, NAT3, PAATOther Designations: N amino acid transporter 3; amino acid transporter system A3Chromosome: 12; Location: 12q13GeneID: 55089 13: SLC25A6 solute carrier family 25 (mitochondrial carrier; adenine nucleotide translocator), member 6 [Homo sapiens]Other Aliases: HGNC:10992, ANT3, ANT3Y, MGC17525Other Designations: ADP,ATP carrier protein, liver isoform T2; ADP/ATP translocase 3; ADP/ATP translocator of liver; adenine nucleotide translocator 3; solute carrier family 25, member A6Chromosome: X, Y; Location: Xp22.32 and YpGeneID: 293 14: SLC2A2 solute carrier family 2 (facilitated glucose transporter), member 2 [Homo sapiens]Other Aliases: HGNC:11006, GLUT2Chromosome: 3; Location: 3q26.1-q26.2GeneID: 6514 15: SLC5A6 solute carrier family 5 (sodium-dependent vitamin transporter), member 6 [Homo sapiens]Other Aliases: HGNC:11041, SMVTChromosome: 2; Location: 2p23GeneID: 8884 16: ABCC3 ATP-binding cassette, sub-family C (CFTR/MRP), member 3 [Homo sapiens]Other Aliases: HGNC:54, ABC31, EST90757, MLP2, MOAT-D, MRP3, cMOAT2Other Designations: ATP-binding cassette, sub-family C, member 3; canicular multispecific organic anion transporterChromosome: 17; Location: 17q22GeneID: 8714 17: LOC387601 putative UST1-like organic anion transporter [Homo sapiens]Chromosome: 11; Location: 11q12.3GeneID: 387601 18: ALDH2 aldehyde dehydrogenase 2 family (mitochondrial) [Homo sapiens]Other Aliases: HGNC:404, ALDH-E2, ALDHI, ALDM, MGC1806Other Designations: ALDH class 2; acetaldehyde dehydrogenase 2; liver mitochondrial ALDH; mitochondrial aldehyde dehydrogenase 2; nucleus-encoded mitochondrial aldehyde dehydrogenase 2Chromosome: 12; Location: 12q24.2GeneID: 217 19: COX7A2 cytochrome c oxidase subunit VIIa polypeptide 2 (liver) [Homo sapiens]Other Aliases: HGNC:2288, COX7AL, COX7AL1, COXVIIa-LOther Designations: hepatic cytochrome-c oxidase chain VIIaChromosome: 6; Location: 6q12GeneID: 1347 20: COX7A3 cytochrome c oxidase subunit VIIa polypeptide 3 (liver) [Homo sapiens]Other Aliases: HGNC:2290, COX7AL, COX7AL2Chromosome: 4; Location: 4q22.3GeneID: 1348 21: ALDH1A1 aldehyde dehydrogenase 1 family, member A1 [Homo sapiens]Other Aliases: HGNC:402, ALDC, ALDH-E1, ALDH1, ALDH11, MGC2318, PUMB1, RALDH1Other Designations: ALDH class 1; acetaldehyde dehydrogenase 1; aldehyde dehydrogenase 1, soluble; aldehyde dehydrogenase 1A1; aldehyde dehydrogenase, liver cytosolic; retinal dehydrogenase 1Chromosome: 9; Location: 9q21.13GeneID: 216 22: PRDX5 peroxiredoxin 5 [Homo sapiens]Other Aliases: HGNC:9355, ACR1, AOEB166, B166, PLP, PMP20, PRDX6, PRXV, SBBI10Other Designations: Alu co-repressor 1; TPx type VI; antioxidant enzyme B166; liver tissue 2D-page spot 71B; peroxisomal antioxidant enzyme; thioredoxin peroxidase PMP20Chromosome: 11; Location: 11q13GeneID: 25824 23: SLC27A2 solute carrier family 27 (fatty acid transporter), member 2 [Homo sapiens]Other Aliases: HGNC:10996, FACVL1, FATP2, HsT17226, VLACS, VLCS, hFACVL1Other Designations: very long-chain fatty-acid-coenzyme A ligase 1; very-long-chain acyl-CoA synthetaseChromosome: 15; Location: 15q21.2GeneID: 11001 24: SLC27A5 solute carrier family 27 (fatty acid transporter), member 5 [Homo sapiens]Other Aliases: HGNC:10999, FACVL3, FATP5, FLJ22987, VLACSR, VLCS-H2, VLCSH2Other Designations: very long-chain acyl-CoA synthetase homolog 2; very long-chain acyl-CoA synthetase-related proteinChromosome: 19; Location: 19q13.43GeneID: 10998 25: ABCG4 ATP-binding cassette, sub-family G (WHITE), member 4 [Homo sapiens]Other Aliases: HGNC:13884, WHITE2Other Designations: ATP-binding cassette, subfamily G, member 4; putative ABC transporterChromosome: 11; Location: 11q23.3GeneID: 64137 26: ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1 [Homo sapiens]Other Aliases: HGNC:40, ABC20, CD243, CLCS, GP170, MDR1, P-gp, PGY1Other Designations: ATP-binding cassette sub-family B member 1; P glycoprotein 1; colchicin sensitivity; doxorubicin resistance; multidrug resistance 1Chromosome: 7; Location: 7q21.1GeneID: 5243 27: AKR1C4 aldo-keto reductase family 1, member C4 (chlordecone reductase; 3-alpha hydroxysteroid dehydrogenase, type I; dihydrodiol dehydrogenase 4) [Homo sapiens]Other Aliases: HGNC:387, 3-alpha-HSD, C11, CDR, CHDR, DD4, HAKRA, MGC22581Other Designations: 3-alpha-hydroxysteroid dehydrogenase variant; aldo-keto reductase family 1, member C4; chlordecone reductase; dihydrodiol dehydrogenase 4; dihydrodiol dehydrogenase isozyme DD4; type I 3-alpha-hydroxysteroid dehydrogenaseChromosome: 10; Location: 10p15-p14GeneID: 1109 28: APOA1 apolipoprotein A-I [Homo sapiens]Other Aliases: HGNC:600Chromosome: 11; Location: 11q23-q24GeneID: 335 29: APOE apolipoprotein E [Homo sapiens]Other Aliases: HGNC:613, AD2, MGC1571Other Designations: Alzheimer disease 2 (APOE*E4-associated, late onset); apolipoprotein E precursor; apolipoprotein E3Chromosome: 19; Location: 19q13.2GeneID: 348 30: NOS2A nitric oxide synthase 2A (inducible, hepatocytes) [Homo sapiens]Other Aliases: HGNC:7873, HEP-NOS, INOS, NOS, NOS2Other Designations: NOS, type II; nitric oxide synthase 2A; nitric oxide synthase, macrophageChromosome: 17; Location: 17q11.2-q12GeneID: 4843 31: ATP5C1 ATP synthase, H+ transporting, mitochondrial F1 complex, gamma polypeptide 1 [Homo sapiens]Other Aliases: HGNC:833, ATP5C, ATP5CL1Other Designations: ATP synthase gamma chain, mitochondrial; ATP synthase, H+ transporting, mitochondrial F1 complex, gamma subunit; mitochondrial ATP synthase, gamma subunit 1Chromosome: 10; Location: 10p15.1GeneID: 509 32: RBP1 retinol binding protein 1, cellular [Homo sapiens]Other Aliases: HGNC:9919, CRABP-I, CRBP, CRBP1, RBPCOther Designations: retinol-binding protein 1, cellularChromosome: 3; Location: 3q23GeneID: 5947 33: STARD4 START domain containing 4, sterol regulated [Homo sapiens]Other Aliases: HGNC:18058Other Designations: START domain containing 4 sterol-regulatedChromosome: 5; Location: 5q22.1GeneID: 134429 34: STARD5 START domain containing 5 [Homo sapiens]Other Aliases: HGNC:18065, MGC10327Other Designations: START domain-containing protein 5; StAR-related lipid transfer protein 5Chromosome: 15; Location: 15q26GeneID: 80765 35: HAAO 3-hydroxyanthranilate 3,4-dioxygenase [Homo sapiens]Other Aliases: HGNC:4796, 3-HAO, HAOChromosome: 2; Location: 2p21GeneID: 23498 36: TNFRSF10B tumor necrosis factor receptor superfamily, member 10b [Homo sapiens]Other Aliases: HGNC:11905, DR5, KILLER, KILLER/DR5, TRAIL-R2, TRAILR2, TRICK2, TRICK2A, TRICK2B, TRICKB, ZTNFR9Other Designations: Fas-like protein precursor; TNF-related apoptosis-inducing ligand receptor 2; TRAIL receptor 2; apoptosis inducing protein TRICK2A/2B; apoptosis inducing receptor TRAIL-R2; cytotoxic TRAIL receptor-2; death domain containing receptor for TRAIL/Apo-2L; death receptor 5; p53-regulated DNA damage-inducible cell death receptor(killer); tumor necrosis factor receptor-like protein ZTNFR9Chromosome: 8; Location: 8p22-p21GeneID: 8795 37: TUSC3 tumor suppressor candidate 3 [Homo sapiens]Other Aliases: HGNC:30242, D8S1992, MGC13453, N33Chromosome: 8; Location: 8p22GeneID: 7991 38: HBG1 hemoglobin, gamma A [Homo sapiens]Other Aliases: HGNC:4831, HBGA, HBGROther Designations: A-gamma globin; Hemoglobin, gamma, regulator of; hemoglobin gamma-a chainChromosome: 11; Location: 11p15.5GeneID: 3047 39: AQP2 aquaporin 2 (collecting duct) [Homo sapiens]Other Aliases: HGNC:634, AQP-CD, MGC34501, WCH-CDOther Designations: aquaporin 2; aquaporin-CD; collecting duct water channel proteinChromosome: 12; Location: 12q12-q13GeneID: 359 40: APOC1 apolipoprotein C-I [Homo sapiens]Other Aliases: HGNC:607Chromosome: 19; Location: 19q13.2GeneID: 341 41: APOB apolipoprotein B (including Ag(x) antigen) [Homo sapiens]Other Aliases: HGNC:603, FLDBOther Designations: apoB-100; apoB-48; apolipoprotein BChromosome: 2; Location: 2p24-p23GeneID: 338 42: ADH7 alcohol dehydrogenase 7 (class IV), mu or sigma polypeptide [Homo sapiens]Other Aliases: HGNC:256, ADH-4Other Designations: Alcohol dehydrogenase-7; class IV alcohol dehydrogenase 7 mu or sigma subunit; gastric alcohol dehydrogenaseChromosome: 4; Location: 4q23-q24GeneID: 131 43: SEC14L3 SEC14-like 3 (S. cerevisiae) [Homo sapiens]Other Aliases: HGNC:18655, TAP2Other Designations: SEC14-like 3; SEC14p-like protein TAP2Chromosome: 22; Location: 22q12.2GeneID: 266629 44: CYGB cytoglobin [Homo sapiens]Other Aliases: HGNC:16505, HGB, STAPOther Designations: histoglobin; stellate cell activation-associated proteinChromosome: 17; Location: 17q25.3GeneID: 114757 45: STARD3 START domain containing 3 [Homo sapiens]Other Aliases: HGNC:17579, CAB1, MLN64, es64Other Designations: steroidogenic acute regulatory protein relatedChromosome: 17; Location: 17q11-q12GeneID: 10948 46: ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11 [Homo sapiens]Other Aliases: HGNC:42, ABC16, BSEP, PFIC-2, PFIC2, PGY4, SPGPOther Designations: ABC member 16, MDR/TAP subfamily; bile salt export pump; progressive familial intrahepatic cholestasis 2Chromosome: 2; Location: 2q24GeneID: 8647 47: APOL1 apolipoprotein L, 1 [Homo sapiens]Other Aliases: HGNC:618, APO-L, APOL, APOL-IOther Designations: apolipoprotein L-I; apolipoprotein L1Chromosome: 22; Location: 22q13.1GeneID: 8542 48: TTR transthyretin (prealbumin, amyloidosis type I) [Homo sapiens]Other Aliases: HGNC:12405, HsT2651, PALB, TBPAOther Designations: prealbumin; transthyretinChromosome: 18; Location: 18q12.1GeneID: 7276 49: PIGR polymeric immunoglobulin receptor [Homo sapiens]Other Aliases: HGNC:8968Other Designations: hepatocellular carcinoma associated protein TB6Chromosome: 1; Location: 1q31-q41GeneID: 5284 50: CYP19A1 cytochrome P450, family 19, subfamily A, polypeptide 1 [Homo sapiens]Other Aliases: HGNC:2594, ARO, ARO1, CPV1, CYAR, CYP19, P-450AROMOther Designations: aromatase; cytochrome P450, family 19; cytochrome P450, subfamily XIX (aromatization of androgens); estrogen synthetase; flavoprotein-linked monooxygenase; microsomal monooxygenaseChromosome: 15; Location: 15q21.1GeneID: 1588 51: APOC4 apolipoprotein C-IV [Homo sapiens]Other Aliases: HGNC:611Chromosome: 19; Location: 19q13.2GeneID: 346 52: ADH6 alcohol dehydrogenase 6 (class V) [Homo sapiens]Other Aliases: HGNC:255, ADH-5Other Designations: aldehyde reductase; class V alcohol dehydrogenase 6Chromosome: 4; Location: 4q23GeneID: 130 53: SLC4A2 solute carrier family 4, anion exchanger, member 2 (erythrocyte membrane protein band 3-like 1) [Homo sapiens]Other Aliases: HGNC:11028, AE2, BND3L, EPB3L1, HKB3, NBND3Chromosome: 7; Location: 7q35-q36GeneID: 6522 54: LIPC lipase, hepatic [Homo sapiens]Other Aliases: HGNC:6619, HL, HTGL, LIPHOther Designations: lipase CChromosome: 15; Location: 15q21-q23GeneID: 3990 55: FABP6 fatty acid binding protein 6, ileal (gastrotropin) [Homo sapiens]Other Aliases: HGNC:3561, I-15P, I-BABP, I-BAP, ILBP, ILBP3, ILLBPOther Designations: gastrotropin; illeal lipid-binding proteinChromosome: 5; Location: 5q33.3-q34GeneID: 2172 56: CYP1B1 cytochrome P450, family 1, subfamily B, polypeptide 1 [Homo sapiens]Other Aliases: HGNC:2597, CP1B, GLC3AOther Designations: aryl hydrocarbon hydroxylase; cytochrome P450, subfamily I (dioxin-inducible), polypeptide 1 (glaucoma 3, primary infantile); flavoprotein-linked monooxygenase; microsomal monooxygenase; xenobiotic monooxygenaseChromosome: 2; Location: 2p21GeneID: 1545 57: COPA coatomer protein complex, subunit alpha [Homo sapiens]Other Aliases: HGNC:2230, HEP-COPOther Designations: alpha coat protein; xeninChromosome: 1; Location: 1q23-q25GeneID: 1314 58: ASPH aspartate beta-hydroxylase [Homo sapiens]Other Aliases: HGNC:757, BAH, CASQ2BP1, HAAH, JCTNOther Designations: aspartyl/asparaginyl-beta-hydroxylase; humbug; junctate; junctin isoform 1; peptide-aspartate beta-dioxygenaseChromosome: 8; Location: 8q12.1GeneID: 444 59: MMP2 matrix metalloproteinase 2 (gelatinase A, 72kDa gelatinase, 72kDa type IV collagenase) [Homo sapiens]Other Aliases: HGNC:7166, CLG4, CLG4A, TBE-1Other Designations: 72kD type IV collagenase; gelatinase A; gelatinase neutrophil; matrix metalloproteinase 2; matrix metalloproteinase 2 (gelatinase A, 72kD gelatinase, 72kD type IV collagenase)Chromosome: 16; Location: 16q13-q21GeneID: 4313 60: IGF1 insulin-like growth factor 1 (somatomedin C) [Homo sapiens]Other Aliases: HGNC:5464, IGFIOther Designations: insulin-like growth factor 1 (somatomedia C)Chromosome: 12; Location: 12q22-q23GeneID: 3479 61: IGF2 insulin-like growth factor 2 (somatomedin A) [Homo sapiens]Other Aliases: HGNC:5466Other Designations: insulin-like growth factor 2; somatomedin AChromosome: 11; Location: 11p15.5GeneID: 3481 62: WT1 Wilms tumor 1 [Homo sapiens]Other Aliases: HGNC:12796, GUD, WAGR, WIT-2, WT33Chromosome: 11; Location: 11p13GeneID: 7490 63: MT2A metallothionein 2A [Homo sapiens]Other Aliases: HGNC:7406, MT2Chromosome: 16; Location: 16q13GeneID: 4502 64: PPARGC1A peroxisome proliferative activated receptor, gamma, coactivator 1, alpha [Homo sapiens]Other Aliases: HGNC:9237, LEM6, PGC-1(alpha), PGC1, PGC1A, PPARGC1Other Designations: PPAR gamma coactivator-1; ligand effect modulator-6; peroxisome proliferative activated receptor gamma coactivator 1Chromosome: 4; Location: 4p15.1GeneID: 10891 65: SP1 Sp1 transcription factor [Homo sapiens]Other Aliases: HGNC:11205Chromosome: 12; Location: 12q13.1GeneID: 6667 66: ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4 [Homo sapiens]Other Aliases: HGNC:45, ABC21, MDR2/3, MDR3, PFIC-3, PGY3Other Designations: ATP-binding cassette, subfamily B, member 4; P glycoprotein 3/multiple drug resistance 3; P-glycoprotein-3/multiple drug resistance-3; multiple drug resistance 3Chromosome: 7; Location: 7q21.1GeneID: 5244