Transporters in the lung:
1: SLC22A18 solute carrier family 22 (organic cation transporter), member 18 [Homo sapiens]Other Aliases: HGNC:10964, BWR1A, BWSCR1A, HET, IMPT1, ITM, ORCTL2, SLC22A1L, TSSC5, p45-BWR1AOther Designations: Beckwith-Wiedemann syndrome chromosome region 1, candidate A; efflux transporter-like protein; imprinted multi-membrane spanning polyspecific transporter-related protein; organic cation transporter-like 2; p45 Beckwith-Wiedemann region 1A; solute carrier family 22 (organic cation transporter), member 1-like; tumor suppressing subtransferable candidate 5; tumor-suppressing STF cDNA 5Chromosome: 11; Location: 11p15.5GeneID: 5002 2: SLC30A9 solute carrier family 30 (zinc transporter), member 9 [Homo sapiens]Other Aliases: HGNC:1329, C4orf1, HUEL, ZNT9Other Designations: chromosome 4 open reading frame 1; expressed in human embryonic lungChromosome: 4; Location: 4p13-p12GeneID: 10463 3: SLC40A1 solute carrier family 40 (iron-regulated transporter), member 1 [Homo sapiens]Other Aliases: HGNC:10909, FPN1, HFE4, IREG1, MTP1, SLC11A3Other Designations: ferroportin 1; iron regulated gene 1; solute carrier family 11 (proton-coupled divalent metal ion transporters), member 3Chromosome: 2; Location: 2q32GeneID: 30061 4: ABCC4 ATP-binding cassette, sub-family C (CFTR/MRP), member 4 [Homo sapiens]Other Aliases: HGNC:55, EST170205, MOAT-B, MOATB, MRP4Other Designations: ATP-binding cassette, sub-family C, member 4; canalicular multispecific organic anion transporter (ABC superfamily)Chromosome: 13; Location: 13q32GeneID: 10257 5: AKR1C1 aldo-keto reductase family 1, member C1 (dihydrodiol dehydrogenase 1; 20-alpha (3-alpha)-hydroxysteroid dehydrogenase) [Homo sapiens]Other Aliases: HGNC:384, 2-ALPHA-HSD, 20-ALPHA-HSD, C9, DD1, DDH, DDH1, H-37, HAKRC, MBAB, MGC8954Other Designations: 20 alpha-hydroxysteroid dehydrogenase; aldo-keto reductase C; aldo-keto reductase family 1, member C1; chlordecone reductase homolog; dihydrodiol dehydrogenase 1; dihydrodiol dehydrogenase isoform DD1; hepatic dihydrodiol dehydrogenase; trans-1,2-dihydrobenzene-1,2-diol dehydrogenase; type II 3-alpha-hydroxysteroid dehydrogenaseChromosome: 10; Location: 10p15-p14GeneID: 1645 6: ABCG2 ATP-binding cassette, sub-family G (WHITE), member 2 [Homo sapiens]Other Aliases: HGNC:74, ABC15, ABCP, BCRP, BCRP1, BMDP, EST157481, MRX, MXR, MXR1Other Designations: ATP-binding cassette, sub-family G, member 2; breast cancer resistance protein; mitoxantrone resistance protein; placenta specific MDR proteinChromosome: 4; Location: 4q22GeneID: 9429 7: 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 8: TXN thioredoxin [Homo sapiens]Other Aliases: HGNC:12435, TRXChromosome: 9; Location: 9q31GeneID: 7295 9: ALDH3A1 aldehyde dehydrogenase 3 family, memberA1 [Homo sapiens]Other Aliases: HGNC:405, ALDH3, ALDHIII, MGC10406Other Designations: ALDH, stomach type; acetaldehyde dehydrogenase; aldehyde dehydrogenase 3 family, member A1; aldehyde dehydrogenase, dimeric NADP-preferringChromosome: 17; Location: 17p11.2GeneID: 218 10: GLRX glutaredoxin (thioltransferase) [Homo sapiens]Other Aliases: HGNC:4330, GRXChromosome: 5; Location: 5q14GeneID: 2745 11: 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 12: TUSC3 tumor suppressor candidate 3 [Homo sapiens]Other Aliases: HGNC:30242, D8S1992, MGC13453, N33Chromosome: 8; Location: 8p22GeneID: 7991 13: NUP98 nucleoporin 98kDa [Homo sapiens]Other Aliases: HGNC:8068, ADIR2, NUP196Other Designations: GLFG-repeat containing nucleoporin; Nup98-Nup96 precursor; nucleoporin 98kDChromosome: 11; Location: 11p15.5GeneID: 4928 14: ADH5 alcohol dehydrogenase 5 (class III), chi polypeptide [Homo sapiens]Other Aliases: HGNC:253, ADH-3, ADHX, FDHOther Designations: Alcohol dehydrogenase (class III), chi polypeptide; class III alcohol dehydrogenase 5 chi subunit; formaldehyde dehydrogenase; glutathione-dependent formaldehyde dehydrogenaseChromosome: 4; Location: 4q21-q25GeneID: 128 15: ADAMTS8 a disintegrin-like and metalloprotease (reprolysin type) with thrombospondin type 1 motif, 8 [Homo sapiens]Other Aliases: HGNC:224, ADAM-TS8, METH2Other Designations: a disintegrin and metalloprotease with thrombospondin motifs-8Chromosome: 11; Location: 11q25GeneID: 11095 16: SFTPA2 surfactant, pulmonary-associated protein A2 [Homo sapiens]Other Aliases: HGNC:10799, COLEC5, SP-A2, SPAIIChromosome: 10; Location: 10q22-q23GeneID: 6436 17: 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 18: 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 19: AMBP alpha-1-microglobulin/bikunin precursor [Homo sapiens]Other Aliases: HGNC:453, HCP, ITI, ITIL, UTIOther Designations: Alpha-1-microglobulin/bikunin precursor (inter-alpha-trypsin inhibitor, light chain; protein HC); Alpha-1-microglobulin/bikunin precursor; inter-alpha-trypsin; alpha-1-microglobulin/bikuninChromosome: 9; Location: 9q32-q33GeneID: 259 20: TXNDC6 thioredoxin domain containing 6 [Homo sapiens]Other Aliases: HGNC:21343, TXL-2Other Designations: thioredoxin-like 2Chromosome: 3; Location: 3q22.3GeneID: 347736 21: AQP3 aquaporin 3 [Homo sapiens]Other Aliases: HGNC:636Chromosome: 9; Location: 9p13GeneID: 360 22: 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 23: 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 24: MIF macrophage migration inhibitory factor (glycosylation-inhibiting factor) [Homo sapiens]Other Aliases: HGNC:7097, GIF, GLIF, MMIFOther Designations: glycosylation-inhibiting factor; phenylpyruvate tautomeraseChromosome: 22; Location: 22q11.23GeneID: 4282 25: CFTR cystic fibrosis transmembrane conductance regulator, ATP-binding cassette (sub-family C, member 7) [Homo sapiens]Other Aliases: HGNC:1884, ABC35, ABCC7, CF, MRP7Other Designations: ATP-binding cassette, sub-family C member 7; CFTR/MRPChromosome: 7; Location: 7q31.2GeneID: 1080 26: SOD1 superoxide dismutase 1, soluble (amyotrophic lateral sclerosis 1 (adult)) [Homo sapiens]Other Aliases: HGNC:11179, ALS, ALS1, IPOAOther Designations: Cu/Zn superoxide dismutase; SOD, soluble; indophenoloxidase A; superoxide dismutase 1, soluble; superoxide dismutase, cystolicChromosome: 21; Location: 21q22.11GeneID: 6647 27: SGK serum/glucocorticoid regulated kinase [Homo sapiens]Other Aliases: HGNC:10810, SGK1Other Designations: serine/threonine protein kinase SGKChromosome: 6; Location: 6q23GeneID: 6446 28: 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 29: OSM oncostatin M [Homo sapiens]Other Aliases: HGNC:8506, MGC20461Chromosome: 22; Location: 22q12.2GeneID: 5008