Transporters in the heart:
1: SLC6A2 solute carrier family 6 (neurotransmitter transporter, noradrenalin), member 2 [Homo sapiens]Other Aliases: HGNC:11048, NAT1, NET, NET1, SLC6A5Other Designations: noradrenaline transporter; norepinephrine transporter; solute carrier family 6 (neurotransmitter transporter, norepinephrine), member 5Chromosome: 16; Location: 16q12.2GeneID: 6530 2: SLC2A1 solute carrier family 2 (facilitated glucose transporter), member 1 [Homo sapiens]Other Aliases: HGNC:11005, GLUT, GLUT1Chromosome: 1; Location: 1p35-p31.3GeneID: 6513 3: SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4 [Homo sapiens]Other Aliases: HGNC:11009, GLUT4Chromosome: 17; Location: 17p13GeneID: 6517 4: CMA1 chymase 1, mast cell [Homo sapiens]Other Aliases: HGNC:2097, CYH, MCT1Other Designations: chymase, heart; chymase, mast cell; mast cell protease IChromosome: 14; Location: 14q11.2GeneID: 1215 5: FABP3 fatty acid binding protein 3, muscle and heart (mammary-derived growth inhibitor) [Homo sapiens]Other Aliases: HGNC:3557, FABP11, H-FABP, MDGI, O-FABPOther Designations: Fatty acid-binding protein 3, muscle; fatty acid binding protein 11; fatty acid binding protein 3; mammary-derived growth inhibitorChromosome: 1; Location: 1p33-p32GeneID: 2170 6: SLC27A6 solute carrier family 27 (fatty acid transporter), member 6 [Homo sapiens]Other Aliases: HGNC:11000, FACVL2, FATP6, VLCS-H1Other Designations: very long-chain acyl-CoA synthetase homolog 1Chromosome: 5; Location: 5q23.3GeneID: 28965 7: ABCA1 ATP-binding cassette, sub-family A (ABC1), member 1 [Homo sapiens]Other Aliases: HGNC:29, ABC1, CERP, HDLDT1, TGDOther Designations: ATP-binding cassette 1; ATP-binding cassette, sub-family A member 1; cholesterol efflux regulatory protein; high density lipoprotein deficiency, Tangier type, 1Chromosome: 9; Location: 9q31.1GeneID: 19 8: GJA1 gap junction protein, alpha 1, 43kDa (connexin 43) [Homo sapiens]Other Aliases: HGNC:4274, CX43, DFNB38, GJAL, ODD, ODDD, ODOD, SDTY3Other Designations: connexin 43; gap junction protein, alpha-like; oculodentodigital dysplasia (syndactyly type III)Chromosome: 6; Location: 6q21-q23.2GeneID: 2697 9: 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 10: SLC8A1 solute carrier family 8 (sodium/calcium exchanger), member 1 [Homo sapiens]Other Aliases: HGNC:11068, NCX1Other Designations: Solute carrier family 8, member 1 (sodium-calcium exchanger-1); solute carrier family 8 (sodium-calcium exchanger), member 1Chromosome: 2; Location: 2p23-p22GeneID: 6546 11: 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 12: APOA1 apolipoprotein A-I [Homo sapiens]Other Aliases: HGNC:600Chromosome: 11; Location: 11q23-q24GeneID: 335 13: LPL lipoprotein lipase [Homo sapiens]Other Aliases: HGNC:6677, LIPDChromosome: 8; Location: 8p22GeneID: 4023 14: 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 15: 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 16: 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 17: 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 18: PDHX pyruvate dehydrogenase complex, component X [Homo sapiens]Other Aliases: HGNC:21350, DLDBP, E3BP, OPDX, PDX1, proXOther Designations: E3-binding protein; pyruvate dehydrogenase complex, lipoyl-containing component XChromosome: 11; Location: 11p13GeneID: 8050 19: TTR transthyretin (prealbumin, amyloidosis type I) [Homo sapiens]Other Aliases: HGNC:12405, HsT2651, PALB, TBPAOther Designations: prealbumin; transthyretinChromosome: 18; Location: 18q12.1GeneID: 7276 20: NOS3 nitric oxide synthase 3 (endothelial cell) [Homo sapiens]Other Aliases: HGNC:7876, ECNOS, eNOSChromosome: 7; Location: 7q36GeneID: 4846 21: APOA4 apolipoprotein A-IV [Homo sapiens]Other Aliases: HGNC:602Chromosome: 11; Location: 11q23GeneID: 337 22: ATP5J ATP synthase, H+ transporting, mitochondrial F0 complex, subunit F6 [Homo sapiens]Other Aliases: HGNC:847, ATP5, ATPM, CF6, F6Other Designations: mitochondrial ATP synthase, coupling factor 6; mitochondrial ATP synthase, subunit F6; mitochondrial ATPase coupling factor 6Chromosome: 21; Location: 21q21.1GeneID: 522 23: PPARG peroxisome proliferative activated receptor, gamma [Homo sapiens]Other Aliases: HGNC:9236, HUMPPARG, NR1C3, PPARG1, PPARG2Other Designations: PPAR gamma; peroxisome proliferative activated receptor gammaChromosome: 3; Location: 3p25GeneID: 5468 24: 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 25: MT2A metallothionein 2A [Homo sapiens]Other Aliases: HGNC:7406, MT2Chromosome: 16; Location: 16q13GeneID: 4502