1: SLCO3A1 
solute carrier organic anion transporter family, member 3A1 [Homo sapiens]Other
Aliases: HGNC:10952, OATP-D, OATP3A1, SLC21A11Other Designations: solute carrier
family 21 (organic anion transporter), member 11Chromosome: 15; Location:
15q26GeneID: 28232
2: SLC30A4 
solute carrier family 30 (zinc transporter), member 4 [Homo sapiens]Other
Aliases: HGNC:11015, ZNT4Chromosome: 15; Location: 15q21.1GeneID: 7782
3: SLC28A1 
solute carrier family 28 (sodium-coupled nucleoside transporter), member 1 [Homo
sapiens]Other Aliases: HGNC:11001, CNT1, HCNT1Chromosome: 15; Location:
15q25-26GeneID: 9154
4: SLC28A2 
solute carrier family 28 (sodium-coupled nucleoside transporter), member 2 [Homo
sapiens]Other Aliases: HGNC:11002, CNT2, HCNT2, HsT17153, SPNT1Chromosome: 15;
Location: 15q15GeneID: 9153
5: RNUT1 
RNA, U transporter 1 [Homo sapiens]Other Aliases: HGNC:14245, KPNBLOther
Designations: snurportin-1Chromosome: 15; Location: 15q23GeneID: 10073
6: OSTbeta 
organic solute transporter beta [Homo sapiens]Chromosome: 15; Location:
15q22.31GeneID: 123264
7: 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
8: LOC440322 
similar to solute carrier family 22 member 4; organic cation transporter 4;
integral membrane transport protein [Homo sapiens]Chromosome: 15; Location:
15p13GeneID: 440322
9: OCA2 
oculocutaneous albinism II (pink-eye dilution homolog, mouse) [Homo
sapiens]Other Aliases: HGNC:8101, BOCA, D15S12, P, PEDOther Designations: P
protein; oculocutaneous albinism II (pink-eye dilution (murine)
homolog)Chromosome: 15; Location: 15q11.2-q12GeneID: 4948
10: RHCG 
Rhesus blood group, C glycoprotein [Homo sapiens]Other Aliases: HGNC:18140,
C15orf6, PDRC2, RHGKOther Designations: Rh type C glycoprotein; chromosome 15
open reading frame 6Chromosome: 15; Location: 15q25GeneID: 51458
11: SLC12A1 
solute carrier family 12 (sodium/potassium/chloride transporters), member 1
[Homo sapiens]Other Aliases: HGNC:10910, BSC1, NKCC2Other Designations: Na-K-2Cl
cotransporter; sodium potassium chloride cotransporter 2Chromosome: 15;
Location: 15q15-q21.1GeneID: 6557
12: SLC12A6 
solute carrier family 12 (potassium/chloride transporters), member 6 [Homo
sapiens]Other Aliases: HGNC:10914, ACCPN, DKFZP434D2135, KCC3, KCC3A, KCC3BOther
Designations: agenesis of corpus callosum and peripheral neuropathy (Andermann
syndrome); potassium chloride cotransporter KCC3Chromosome: 15; Location:
15q13-q15GeneID: 9990
13: 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
14: VPS33B 
vacuolar protein sorting 33B (yeast) [Homo sapiens]Other Aliases: HGNC:12712,
FLJ14848Other Designations: vacuolar protein sorting 33B (yeast homolog);
vacuolar protein sorting 33B (yeast homolog))Chromosome: 15; Location:
15q26.1GeneID: 26276
15: SV2B 
synaptic vesicle glycoprotein 2B [Homo sapiens]Other Aliases: HGNC:16874,
HsT19680, KIAA0735Other Designations: synaptic vesicle protein 2B
homologChromosome: 15; Location: 15q26.1GeneID: 9899
16: COX5A 
cytochrome c oxidase subunit Va [Homo sapiens]Other Aliases: HGNC:2267, COX,
COX-VA, VAOther Designations: cytochrome c oxidase polypeptide, mitochondrial
precursorChromosome: 15; Location: 15q25GeneID: 9377
17: AP3B2 
adaptor-related protein complex 3, beta 2 subunit [Homo sapiens]Other Aliases:
HGNC:567, NAPTBOther Designations: Neuronal adaptin-like protein,
beta-subunitChromosome: 15; Location: 15qGeneID: 8120
18: RLBP1 
retinaldehyde binding protein 1 [Homo sapiens]Other Aliases: HGNC:10024, CRALBP,
MGC3663Other Designations: Newfoundland rod-cone dystrophy, included; cellular
retinaldehyde-binding protein-1; retinaldehyde-binding protein 1Chromosome: 15;
Location: 15q26GeneID: 6017
19: PTPN9 
protein tyrosine phosphatase, non-receptor type 9 [Homo sapiens]Other Aliases:
HGNC:9661, MEG2Other Designations: PTPase-MEG2; protein-tyrosine phosphatase
MEG2Chromosome: 15; Location: 15q23GeneID: 5780
20: LOXL1 
lysyl oxidase-like 1 [Homo sapiens]Other Aliases: HGNC:6665, LOXLChromosome: 15;
Location: 15q22GeneID: 4016
21: GABRA5 
gamma-aminobutyric acid (GABA) A receptor, alpha 5 [Homo sapiens]Other Aliases:
HGNC:4079Chromosome: 15; Location: 15q11.2-q12GeneID: 2558
22: CYP11A1 
cytochrome P450, family 11, subfamily A, polypeptide 1 [Homo sapiens]Other
Aliases: HGNC:2590, CYP11A, P450SCCOther Designations: cholesterol 20-22
desmolase; cholesterol monooxygenase (side-chain cleaving); cytochrome P450,
subfamily XIA; cytochrome P450, subfamily XIA (cholesterol side chain cleavage);
cytochrome P450C11A1; steroid 20-22-lyaseChromosome: 15; Location:
15q23-q24GeneID: 1583
23: CYP1A2 
cytochrome P450, family 1, subfamily A, polypeptide 2 [Homo sapiens]Other
Aliases: HGNC:2596, CP12, P3-450, P450(PA)Other Designations: P450 form 4; aryl
hydrocarbon hydroxylase; cytochrome P450, subfamily I (aromatic
compound-inducible), polypeptide 2; dioxin-inducible P3-450; flavoprotein-linked
monooxygenase; microsomal monooxygenase; xenobiotic monooxygenaseChromosome: 15;
Location: 15q22-qterGeneID: 1544
24: CHRNA3 
cholinergic receptor, nicotinic, alpha polypeptide 3 [Homo sapiens]Other
Aliases: HGNC:1957Other Designations: Cholinergic receptor, neuronal nicotinic,
alpha polypeptide-3Chromosome: 15; Location: 15q24GeneID: 1136
25: ALDH1A2 
aldehyde dehydrogenase 1 family, member A2 [Homo sapiens]Other Aliases:
HGNC:15472, MGC26444, RALDH(II), RALDH2, RALDH2-TOther Designations: aldehyde
dehydrogenase 1A2; retinaldehyde dehydrogenase 2; retinaldehyde-specific
dehydrogenase type 2Chromosome: 15; Location: 15q21.3GeneID: 8854
26: GRP58 
glucose regulated protein, 58kDa [Homo sapiens]Other Aliases: HGNC:4606, ERp57,
ERp60, ERp61, GRP57, HsT17083, P58, PI-PLCChromosome: 15; Location: 15q15GeneID:
2923
27: 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
28: CRABP1 
cellular retinoic acid binding protein 1 [Homo sapiens]Other Aliases: HGNC:2338,
CRABP, CRABP-I, CRABPI, RBP5Other Designations: cellular retinoic acid-binding
protein 1Chromosome: 15; Location: 15q24GeneID: 1381
29: SNX1 
sorting nexin 1 [Homo sapiens]Other Aliases: HGNC:11172, HsT17379, MGC8664,
SNX1AOther Designations: sorting nexin 1AChromosome: 15; Location:
15q22.31GeneID: 6642
30: LIPC 
lipase, hepatic [Homo sapiens]Other Aliases: HGNC:6619, HL, HTGL, LIPHOther
Designations: lipase CChromosome: 15; Location: 15q21-q23GeneID: 3990
31: CHRNB4 
cholinergic receptor, nicotinic, beta polypeptide 4 [Homo sapiens]Other Aliases:
HGNC:1964Other Designations: Cholinergic receptor, neuronal nicotinic, beta
polypeptide-4Chromosome: 15; Location: 15q24GeneID: 1143
32: AQP9 
aquaporin 9 [Homo sapiens]Other Aliases: HGNC:643, HsT17287, SSC1Chromosome: 15;
Location: 15q22.1-22.2GeneID: 366
33: DUOX1 
dual oxidase 1 [Homo sapiens]Other Aliases: HGNC:3062, LNOX1, NOXEF1, THOX1Other
Designations: NADPH thyroid oxidase 1; flavoprotein NADPH oxidase; nicotinamide
adenine dinucleotide phosphate oxidaseChromosome: 15; Location: 15q15.3GeneID:
53905
34: DUOX2 
dual oxidase 2 [Homo sapiens]Other Aliases: HGNC:13273, LNOX2, NOXEF2, P138-TOX,
THOX2Other Designations: NADH/NADPH thyroid oxidase p138-tox; NADPH
oxidase/peroxidase DUOX2; NADPH thyroid oxidase 2; dual oxidase-like domains 2;
flavoprotein NADPH oxidase; nicotinamide adenine dinucleotide phosphate
oxidaseChromosome: 15; Location: 15q15.3GeneID: 50506
35: NIPA1 
non imprinted in Prader-Willi/Angelman syndrome 1 [Homo sapiens]Other Aliases:
HGNC:17043, FSP3, MGC35570, SPG6Other Designations: non-imprinted in
Prader-Willi/Angelman syndrome 1; spastic paraplegia 6 (autosomal
dominant)Chromosome: 15; Location: 15q11.2GeneID: 123606