1: 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
2: SLC2A3 
solute carrier family 2 (facilitated glucose transporter), member 3 [Homo
sapiens]Other Aliases: HGNC:11007, GLUT3Other Designations: GLUCOSE TRANSPORTER
TYPE 3, BRAINChromosome: 12; Location: 12p13.3GeneID: 6515
3: SLCO1B1 
solute carrier organic anion transporter family, member 1B1 [Homo sapiens]Other
Aliases: HGNC:10959, LST-1, OATP-C, OATP1B1, OATP2, SLC21A6Other Designations:
solute carrier family 21 (organic anion transporter), member 6Chromosome: 12;
Location: 12pGeneID: 10599
4: SLCO1B3 
solute carrier organic anion transporter family, member 1B3 [Homo sapiens]Other
Aliases: HGNC:10961, OATP1B3, OATP8, SLC21A8Other Designations: solute carrier
family 21 (organic anion transporter), member 8Chromosome: 12; Location:
12p12GeneID: 28234
5: SLC2A14 
solute carrier family 2 (facilitated glucose transporter), member 14 [Homo
sapiens]Other Aliases: HGNC:18301, GLUT14Other Designations: glucose transporter
14Chromosome: 12; Location: 12p13.31GeneID: 144195
6: SLC5A8 
solute carrier family 5 (iodide transporter), member 8 [Homo sapiens]Other
Aliases: HGNC:19119, AITOther Designations: apical iodide transporterChromosome:
12; Location: 12q23.3GeneID: 160728
7: SLC6A12 
solute carrier family 6 (neurotransmitter transporter, betaine/GABA), member 12
[Homo sapiens]Other Aliases: HGNC:11045, BGT-1, BGT1Other Designations:
gamma-aminobutyric acid transporterChromosome: 12; Location: 12p13GeneID: 6539
8: SLCO1C1 
solute carrier organic anion transporter family, member 1C1 [Homo sapiens]Other
Aliases: HGNC:13819, OATP-F, OATP1, OATP1C1, SLC21A14Other Designations: solute
carrier family 21 (organic anion transporter), member 14Chromosome: 12;
Location: 12p12.3GeneID: 53919
9: SLC38A2 
solute carrier family 38, member 2 [Homo sapiens]Other Aliases: HGNC:13448,
ATA2, KIAA1382, PRO1068, SAT2, SNAT2Other Designations: amino acid transporter
2; system A amino acid transporterChromosome: 12; Location: 12qGeneID: 54407
10: 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
11: SLC6A15 
solute carrier family 6 (neurotransmitter transporter), member 15 [Homo
sapiens]Other Aliases: HGNC:13621, FLJ10316, MGC87066, NTT73, V7-3, hv7-3Other
Designations: homolog of rat orphan transporter v7-3Chromosome: 12; Location:
12q21.3GeneID: 55117
12: SLC38A1 
solute carrier family 38, member 1 [Homo sapiens]Other Aliases: HGNC:13447,
ATA1, NAT2, SAT1, SNAT1Other Designations: amino acid transporter system
A1Chromosome: 12; Location: 12q13.11GeneID: 81539
13: SLC2A13 
solute carrier family 2 (facilitated glucose transporter), member 13 [Homo
sapiens]Other Aliases: HGNC:15956, HMITOther Designations: proton (H+)
myo-inositol symporterChromosome: 12; Location: 12q12GeneID: 114134
14: SLC39A5 
solute carrier family 39 (metal ion transporter), member 5 [Homo sapiens]Other
Aliases: HGNC:20502, LZT-Hs7, MGC34778Chromosome: 12; Location: 12q13.3GeneID:
283375
15: SLC17A8 
solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter),
member 8 [Homo sapiens]Other Aliases: HGNC:20151, VGLUT3Other Designations:
vesicular glutamate transporter 3Chromosome: 12; Location: 12q23.1GeneID: 246213
16: SLC16A7 
solute carrier family 16 (monocarboxylic acid transporters), member 7 [Homo
sapiens]Other Aliases: HGNC:10928, MCT2Other Designations: monocarboxylate
transporter 2; solute carrier family 16, member 7Chromosome: 12; Location:
12q13GeneID: 9194
17: SLC15A4 
solute carrier family 15, member 4 [Homo sapiens]Other Aliases: HGNC:23090,
PHT1, PTR4Other Designations: peptide-histidine transporter 4Chromosome: 12;
Location: 12q24.32GeneID: 121260
18: SLC6A13 
solute carrier family 6 (neurotransmitter transporter, GABA), member 13 [Homo
sapiens]Other Aliases: HGNC:11046, GAT-2, GAT2Other Designations: GABA transport
proteinChromosome: 12; Location: 12p13.3GeneID: 6540
19: LST-3 
liver-specific organic anion transporter 3 [Homo sapiens]Chromosome: 12;
Location: 12p12.3GeneID: 338821
20: SLC2A3P3 
solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 3
[Homo sapiens]Other Aliases: HGNC:31075Chromosome: 12; Location: 12p13.3GeneID:
399494
21: SLC11A2 
solute carrier family 11 (proton-coupled divalent metal ion transporters),
member 2 [Homo sapiens]Other Aliases: HGNC:10908, DCT1, DMT1, NRAMP2Other
Designations: natural resistance-associated macrophage protein 2Chromosome: 12;
Location: 12q13GeneID: 4891
22: ABCB9 
ATP-binding cassette, sub-family B (MDR/TAP), member 9 [Homo sapiens]Other
Aliases: HGNC:50, EST122234, KIAA1520, TAPLChromosome: 12; Location:
12q24GeneID: 23457
23: ABCD2 
ATP-binding cassette, sub-family D (ALD), member 2 [Homo sapiens]Other Aliases:
HGNC:66, ABC39, ALDL1, ALDR, ALDRP, hALDROther Designations: ATP-binding
cassette, sub-family D, member 2; adrenoleukodystrophy-like 1Chromosome: 12;
Location: 12q11-q12GeneID: 225
24: NUP107 
nucleoporin 107kDa [Homo sapiens]Other Aliases: HGNC:29914, NUP84Other
Designations: nuclear pore complex proteinChromosome: 12; Location: 12q15GeneID:
57122
25: DAP13 
13kDa differentiation-associated protein [Homo sapiens]Other Designations: NADH:
ubiquinone oxidoreductaseChromosome: 12; Location: 12q22GeneID: 55967
26: RPH3A 
rabphilin 3A homolog (mouse) [Homo sapiens]Other Aliases: HGNC:17056, KIAA0985,
rabphilinOther Designations: rabphilin 3A homologChromosome: 12; Location:
12q24.13GeneID: 22895
27: IPO8 
importin 8 [Homo sapiens]Other Aliases: HGNC:9853, RANBP8Other Designations: RAN
binding protein 8; RAN-binding protein 8Chromosome: 12; Location:
12p11.21GeneID: 10526
28: PAMCI 
peptidylglycine alpha-amidating monooxygenase COOH-terminal interactor [Homo
sapiens]Other Aliases: HGNC:15739, P-CIP1Other Designations: peptidylglycine
alpha-amidating monooxygenase COOH-terminal interactor protein-1Chromosome: 12;
Location: 12q21.31GeneID: 9182
29: RODH 
3-hydroxysteroid epimerase [Homo sapiens]Other Aliases: HSEOther Designations:
3(alpha->beta)-hydroxysteroid epimerase; NAD+ -dependent 3 alpha-hydroxysteroid
dehydrogenase; oxidative 3-alpha-hydroxysteroid-dehydrogenase; oxidoreductase;
retinol dehydrogenaseChromosome: 12; Location: 12q13GeneID: 8630
30: SYT1 
synaptotagmin I [Homo sapiens]Other Aliases: HGNC:11509, P65, SVP65, SYTOther
Designations: synaptotagmin 1Chromosome: 12; Location: 12cen-q21GeneID: 6857
31: EPIM 
epimorphin [Homo sapiens]Other Aliases: HGNC:3403, MGC51014, STX2A, STX2B,
STX2COther Designations: syntaxin 2Chromosome: 12; Location: 12q24.33GeneID:
2054
32: DAO 
D-amino-acid oxidase [Homo sapiens]Other Aliases: HGNC:2671, DAAO, DAMOX,
MGC35381, OXDAChromosome: 12; Location: 12q24GeneID: 1610
33: ATP5B 
ATP synthase, H+ transporting, mitochondrial F1 complex, beta polypeptide [Homo
sapiens]Other Aliases: HGNC:830, ATPMB, ATPSB, MGC5231Other Designations: ATP
synthase, H+ transporting, mitochondrial F1 complex, beta subunit; mitochondrial
ATP synthetase, beta subunitChromosome: 12; Location: 12q13.13GeneID: 506
34: AQP5 
aquaporin 5 [Homo sapiens]Other Aliases: HGNC:638Other Designations:
Aquaporin-5Chromosome: 12; Location: 12q13GeneID: 362
35: 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
36: RBP5 
retinol binding protein 5, cellular [Homo sapiens]Other Aliases: HGNC:15847,
CRBP-III, CRBP3, CRBPIIIOther Designations: putative cellular retinol-binding
protein CRBP III; retinol-binding protein 5, cellularChromosome: 12; Location:
12p13.31GeneID: 83758
37: FLJ20436 
hypothetical protein FLJ20436 [Homo sapiens]Other Aliases: FLJ12670Chromosome:
12; Location: 12q13.11GeneID: 54934
38: ATP6V0A2 
ATPase, H+ transporting, lysosomal V0 subunit a isoform 2 [Homo sapiens]Other
Aliases: HGNC:18481, ATP6N1D, ATP6a2, J6B7, Stv1, TJ6, TJ6M, TJ6s, Vph1, a2Other
Designations: infantile malignant osteopetrosisChromosome: 12; Location:
12q24.31GeneID: 23545
39: ABCC9 
ATP-binding cassette, sub-family C (CFTR/MRP), member 9 [Homo sapiens]Other
Aliases: HGNC:60, ABC37, SUR2Other Designations: ATP-binding cassette,
sub-family C, member 9; sulfonylurea receptor 2AChromosome: 12; Location:
12p12.1GeneID: 10060
40: KIAA0528 
KIAA0528 gene product [Homo sapiens]Chromosome: 12; Location: 12p12.1GeneID:
9847
41: RODH-4 
microsomal NAD+-dependent retinol dehydrogenase 4 [Homo sapiens]Chromosome: 12;
Location: 12q13.3GeneID: 8608
42: KCNA1 
potassium voltage-gated channel, shaker-related subfamily, member 1 (episodic
ataxia with myokymia) [Homo sapiens]Other Aliases: HGNC:6218, AEMK, EA1, HUK1,
KV1.1, MBK1, MK1, RBK1Other Designations: Potassium voltage-gated channel,
shaker-related subfamily, member 1; potassium voltage-gated channel,
shaker-related subfamily, member 1Chromosome: 12; Location: 12p13GeneID: 3736
43: ITPR2 
inositol 1,4,5-triphosphate receptor, type 2 [Homo sapiens]Other Aliases:
HGNC:6181, IP3R2Chromosome: 12; Location: 12p11GeneID: 3709
44: ATP5G2 
ATP synthase, H+ transporting, mitochondrial F0 complex, subunit c (subunit 9),
isoform 2 [Homo sapiens]Other Aliases: HGNC:842Other Designations: ATP synthase
lipid-binding protein, mitochondrial; ATP synthase proteolipid P2; ATP synthase,
H+ transporting, mitochondrial F0 complex, subunit c; ATPase protein 9; ATPase
subunit C; mitochondrial ATP synthase, subunit C (subunit 9), isoform
2Chromosome: 12; Location: 12q13.13GeneID: 517
45: APOF 
apolipoprotein F [Homo sapiens]Other Aliases: HGNC:615, Apo-F,
MGC22520Chromosome: 12; Location: 12q13.3GeneID: 319
46: 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
47: SLC41A2 
solute carrier family 41, member 2 [Homo sapiens]Other Aliases: HGNC:31045,
DKFZP434K0427, SLC41A1-L1Other Designations: SLC41A1-like 1Chromosome: 12;
Location: 12q23.3GeneID: 84102
48: VPS33A 
vacuolar protein sorting 33A (yeast) [Homo sapiens]Other Aliases: HGNC:18179,
FLJ22395, FLJ23187Other Designations: vacuolar protein sorting 33AChromosome:
12; Location: 12q24.31GeneID: 65082
49: DKFZp761H039 
hypothetical protein DKFZp761H039 [Homo sapiens]Chromosome: 12; Location:
12q24.11GeneID: 55530
50: RACGAP1 
Rac GTPase activating protein 1 [Homo sapiens]Other Aliases: HGNC:9804, ID-GAP,
MgcRacGAPOther Designations: GTPase activating proteinChromosome: 12; Location:
12q13.12GeneID: 29127
51: NOS1 
nitric oxide synthase 1 (neuronal) [Homo sapiens]Other Aliases: HGNC:7872,
NOSChromosome: 12; Location: 12q24.2-q24.31GeneID: 4842
52: MIP 
major intrinsic protein of lens fiber [Homo sapiens]Other Aliases: HGNC:7103,
AQP0, LIM1, MIP26, MP26Other Designations: aquaporinChromosome: 12; Location:
12q13GeneID: 4284
53: M6PR 
mannose-6-phosphate receptor (cation dependent) [Homo sapiens]Other Aliases:
HGNC:6752, CD-MPR, MPR46, SMPROther Designations: 46-kDa mannose 6-phosphate
receptor; Mr 46,000 Man6PR; cation-dependent mannose-6-phosphate
receptorChromosome: 12; Location: 12p13GeneID: 4074
54: LRP1 
low density lipoprotein-related protein 1 (alpha-2-macroglobulin receptor) [Homo
sapiens]Other Aliases: HGNC:6692, A2MR, APOER, APR, CD91, LRPOther Designations:
alpha-2-macroglobulin receptor; low density lipoprotein-related protein
1Chromosome: 12; Location: 12q13-q14GeneID: 4035
55: KIF5A 
kinesin family member 5A [Homo sapiens]Other Aliases: HGNC:6323, D12S1889,
MY050, NKHC, SPG10Other Designations: kinesin, heavy chain, neuron-specific;
spastic paraplegia 10 (autosomal dominant)Chromosome: 12; Location:
12q13.13GeneID: 3798
56: GRIN2B 
glutamate receptor, ionotropic, N-methyl D-aspartate 2B [Homo sapiens]Other
Aliases: HGNC:4586, NMDAR2B, NR2B, hNR3Other Designations: N-methyl-D-aspartate
receptor subunit 2BChromosome: 12; Location: 12p12GeneID: 2904
57: GOLGA3 
golgi autoantigen, golgin subfamily a, 3 [Homo sapiens]Other Aliases: HGNC:4426,
GCP170, MEA-2Other Designations: Golgi autoantigen, golgin subfamily a, 3; Golgi
complex-associated protein of 170 kD; Golgi membrane associated protein; Golgi
peripheral membrane protein; SY2/SY10 protein; golgin-160; golgin-165; male
enhanced antigen-2Chromosome: 12; Location: 12q24.33GeneID: 2802
58: AQP6 
aquaporin 6, kidney specific [Homo sapiens]Other Aliases: HGNC:639, AQP2LOther
Designations: Aquaporin-6, kidney specific; aquaporin 2-like, kidney specific;
aquaporin 6Chromosome: 12; Location: 12q13GeneID: 363
59: NR1H4 
nuclear receptor subfamily 1, group H, member 4 [Homo sapiens]Other Aliases:
HGNC:7967, BAR, FXR, HRR-1, HRR1, RIP14Chromosome: 12; Location: 12q23.1GeneID:
9971
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: A2M 
alpha-2-macroglobulin [Homo sapiens]Other Aliases: HGNC:7Chromosome: 12;
Location: 12p13.3-p12.3GeneID: 2
62: SP1 
Sp1 transcription factor [Homo sapiens]Other Aliases: HGNC:11205Chromosome: 12;
Location: 12q13.1GeneID: 6667
63: TAPBPL 
TAP binding protein-like [Homo sapiens]Other Aliases: HGNC:30683, FLJ10143,
TAPBP-R, TAPBPROther Designations: TAP binding protein relatedChromosome: 12;
Location: 12p13.31GeneID: 55080