1: SLCO5A1 
solute carrier organic anion transporter family, member 5A1 [Homo sapiens]Other
Aliases: HGNC:19046, OATP-J, OATP5A1, OATPRP4, SLC21A15Other Designations:
organic anion transporter polypeptide-related protein 4; solute carrier family
21 (organic anion transporter), member 15Chromosome: 8; Location: 8q13.3GeneID:
81796
2: SLC7A2 
solute carrier family 7 (cationic amino acid transporter, y+ system), member 2
[Homo sapiens]Other Aliases: HGNC:11060, ATRC2, CAT-2, HCAT2Other Designations:
amino acid transporter, cationic 2Chromosome: 8; Location: 8p22-p21.3GeneID:
6542
3: SLC7A13 
solute carrier family 7, (cationic amino acid transporter, y+ system) member 13
[Homo sapiens]Other Aliases: HGNC:23092, AGT-1, AGT1, XAT2Other Designations:
amino acid transporter XAT2Chromosome: 8; Location: 8q21.3GeneID: 157724
4: SLC39A14 
solute carrier family 39 (zinc transporter), member 14 [Homo sapiens]Other
Aliases: HGNC:20858, KIAA0062, LZT-Hs4Other Designations: solute carrier family
39 (metal ion transporter), member 14Chromosome: 8; Location: 8p21.3GeneID:
23516
5: SLC30A8 
solute carrier family 30 (zinc transporter), member 8 [Homo sapiens]Other
Aliases: HGNC:20303, ZnT-8Other Designations: zinc transporter ZnT-8Chromosome:
8; Location: 8q24.11GeneID: 169026
6: 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
7: SLC39A4 
solute carrier family 39 (zinc transporter), member 4 [Homo sapiens]Other
Aliases: HGNC:17129, AEZ, FLJ20327, ZIP4Other Designations: acrodermatitis
enteropathica, zinc-deficiency typeChromosome: 8; Location: 8q24.3GeneID: 55630
8: SLC26A7 
solute carrier family 26, member 7 [Homo sapiens]Other Aliases: HGNC:14467,
SUT2Other Designations: sulfate anion transporterChromosome: 8; Location:
8q23GeneID: 115111
9: SLC20A2 
solute carrier family 20 (phosphate transporter), member 2 [Homo sapiens]Other
Aliases: HGNC:10947, GLVR2, Glvr-2, MLVAR, PIT-2Other Designations: gibbon ape
leukemia virus receptor 2; murine leukemia virus, amphotropic, receptor for;
solute carrier family 20, member 2Chromosome: 8; Location: 8p12-q21GeneID: 6575
10: SLC2A3P4 
solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 4
[Homo sapiens]Other Aliases: HGNC:31076Chromosome: 8; Location: 8q21.3GeneID:
399495
11: LAPTM4B 
lysosomal associated protein transmembrane 4 beta [Homo sapiens]Other Aliases:
HGNC:13646, LAPTM4beta, LC27Other Designations: lysosomal-associated
transmembrane protein 4 beta; putative integral membrane transporterChromosome:
8; Location: 8q22.1GeneID: 55353
12: SLC18A1 
solute carrier family 18 (vesicular monoamine), member 1 [Homo sapiens]Other
Aliases: HGNC:10934, CGAT, VAT1, VMAT1Chromosome: 8; Location: 8p21.3GeneID:
6570
13: MFTC 
mitochondrial folate transporter/carrier [Homo sapiens]Chromosome: 8; Location:
8q22.3GeneID: 81034
14: XPO7 
exportin 7 [Homo sapiens]Other Aliases: HGNC:14108, KIAA0745, RANBP16Other
Designations: RAN binding protein 16Chromosome: 8; Location: 8p21GeneID: 23039
15: 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
16: TUSC3 
tumor suppressor candidate 3 [Homo sapiens]Other Aliases: HGNC:30242, D8S1992,
MGC13453, N33Chromosome: 8; Location: 8p22GeneID: 7991
17: TTPA 
tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E
deficiency) [Homo sapiens]Other Aliases: HGNC:12404, AVED, TTP1Other
Designations: Tocopherol (alpha) transfer proteinChromosome: 8; Location:
8q13.1-q13.3GeneID: 7274
18: STAR 
steroidogenic acute regulator [Homo sapiens]Other Aliases: HGNC:11359,
STARD1Other Designations: START domain containing 1; steroidogenic acute
regulatory proteinChromosome: 8; Location: 8p11.2GeneID: 6770
19: PMP2 
peripheral myelin protein 2 [Homo sapiens]Other Aliases: HGNC:9117, FABP8,
M-FABP, MP2, P2Chromosome: 8; Location: 8q21.3-q22.1GeneID: 5375
20: MSR1 
macrophage scavenger receptor 1 [Homo sapiens]Other Aliases: HGNC:7376, SCARA1,
SR-A, phSR1, phSR2Other Designations: macrophage acetylated LDL receptor I and
II; macrophage scavenger receptor type III; scavenger receptor class A, member
1Chromosome: 8; Location: 8p22GeneID: 4481
21: INDO 
indoleamine-pyrrole 2,3 dioxygenase [Homo sapiens]Other Aliases: HGNC:6059,
CD107B, IDOOther Designations: Indoleamine 2,3-dioxygenase; indole
2,3-dioxygenaseChromosome: 8; Location: 8p12-p11GeneID: 3620
22: FABP5 
fatty acid binding protein 5 (psoriasis-associated) [Homo sapiens]Other Aliases:
HGNC:3560, E-FABP, EFABP, PA-FABP, PAFABPChromosome: 8; Location: 8q21.13GeneID:
2171
23: CHRNB3 
cholinergic receptor, nicotinic, beta polypeptide 3 [Homo sapiens]Other Aliases:
HGNC:1963Chromosome: 8; Location: 8p11.2GeneID: 1142
24: MGC34646 
hypothetical protein MGC34646 [Homo sapiens]Chromosome: 8; Location:
8q12.2-q12.3GeneID: 157807
25: FBXO32 
F-box protein 32 [Homo sapiens]Other Aliases: HGNC:16731, ATROGIN1, FLJ32424,
Fbx32, MAFbx, MGC33610Other Designations: F-box only protein 32; atrogin-1;
muscle atrophy F-box proteinChromosome: 8; Location: 8q24.13GeneID: 114907
26: TRPA1 
transient receptor potential cation channel, subfamily A, member 1 [Homo
sapiens]Other Aliases: HGNC:497, ANKTM1Other Designations: ankyrin-like protein
1; ankyrin-like with transmembrane domains 1Chromosome: 8; Location: 8q13GeneID:
8989
27: TSTA3 
tissue specific transplantation antigen P35B [Homo sapiens]Other Aliases:
HGNC:12390, FX, P35BOther Designations: 3-5 epimerase/4-reductase;
GDP-4-keto-6-deoxy-D-mannose epimerase-reductase; Tissue-specific
transplantation antigen-3; tissue specific transplantation antigen 3Chromosome:
8; Location: 8q24.3GeneID: 7264
28: FABP4 
fatty acid binding protein 4, adipocyte [Homo sapiens]Other Aliases: HGNC:3559,
A-FABPChromosome: 8; Location: 8q21GeneID: 2167
29: CYC1 
cytochrome c-1 [Homo sapiens]Other Aliases: HGNC:2579Chromosome: 8; Location:
8q24.3GeneID: 1537
30: CPNE3 
copine III [Homo sapiens]Other Aliases: HGNC:2316, CPN3, KIAA0636,
PRO1071Chromosome: 8; Location: 8q21.3GeneID: 8895
31: LPL 
lipoprotein lipase [Homo sapiens]Other Aliases: HGNC:6677, LIPDChromosome: 8;
Location: 8p22GeneID: 4023
32: LOXL2 
lysyl oxidase-like 2 [Homo sapiens]Other Aliases: HGNC:6666, WS9-14Chromosome:
8; Location: 8p21.3-p21.2GeneID: 4017
33: ATP6V1C1 
ATPase, H+ transporting, lysosomal 42kDa, V1 subunit C, isoform 1 [Homo
sapiens]Other Aliases: HGNC:856, ATP6C, ATP6D, FLJ20057, VATC, Vma5Other
Designations: ATPase, H+ transporting, lysosomal (vacuolar proton pump) 42kD;
ATPase, H+ transporting, lysosomal 42kD, V1 subunit C, isoform 1; ATPase, H+
transporting, lysosomal, 42kD; ATPase, H+ transporting, lysosomal, subunit C;
H(+)-transporting two-sector ATPase, subunit C; H+ -ATPase C subunit;
H+-transporting ATPase chain C, vacuolar; V-ATPase C subunit; vacuolar ATP
synthase subunit C; vacuolar proton pump C subunit; vacuolar proton pump, 42-kD
subunit; vacuolar proton-ATPase, subunit C, VI domain; vat cChromosome: 8;
Location: 8q22.3GeneID: 528
34: 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