1: TAP2 
transporter 2, ATP-binding cassette, sub-family B (MDR/TAP) [Homo sapiens]Other
Aliases: HGNC:44, ABC18, ABCB3, APT2, D6S217E, PSF2, RING11Other Designations:
ABC transporter, MHC 2; ATP-binding cassette, sub-family B (MDR/TAP), member 3;
antigen peptide transporter 2; peptide supply factor 2; peptide transporter
PSF2; transporter 2, ABC (ATP binding cassette); transporter 2, ATP-binding
cassette, sub-family BChromosome: 6; Location: 6p21.3GeneID: 6891
2: TAP1 
transporter 1, ATP-binding cassette, sub-family B (MDR/TAP) [Homo sapiens]Other
Aliases: HGNC:43, ABC17, ABCB2, APT1, D6S114E, PSF1, RING4Other Designations:
ABC transporter, MHC 1; ATP-binding cassette, sub-family B (MDR/TAP), member 2;
ATP-binding cassette, sub-family B, member 2; antigen peptide transporter 1;
peptide supply factor 1; transporter 1, ATP-binding cassette, sub-family B;
transporter, ATP-binding cassette, major histocompatibility complex,
1Chromosome: 6; Location: 6p21.3GeneID: 6890
3: SLC22A16 
solute carrier family 22 (organic cation transporter), member 16 [Homo
sapiens]Other Aliases: HGNC:20302, CT2, FLIPT2, OCT6, OKB1, dJ261K5.1Other
Designations: carnitine transporter 2; fly-like putative organic ion transporter
2; organic cation transporter 6; solute carrier family 22, member 16Chromosome:
6; Location: 6q21-q22.1GeneID: 85413
4: SLC35A1 
solute carrier family 35 (CMP-sialic acid transporter), member A1 [Homo
sapiens]Other Aliases: HGNC:11021, CMPST, CST, hCST, inactiveOther Designations:
mutated CMP-sialic acid transporter A1; solute carrier family 35 (CMP-sialic
acid transporter), member 1; solute carrier family 35 (UDP-galactose
transporter), member 1Chromosome: 6; Location: 6q15GeneID: 10559
5: SLC22A3 
solute carrier family 22 (extraneuronal monoamine transporter), member 3 [Homo
sapiens]Other Aliases: HGNC:10967, EMT, EMTH, OCT3Other Designations: EMT
organic cation transporter 3; extraneuronal monoamine transporter; organic
cation transporter 3; solute carrier family 22 member 3Chromosome: 6; Location:
6q26-q27GeneID: 6581
6: SLC22A7 
solute carrier family 22 (organic anion transporter), member 7 [Homo
sapiens]Other Aliases: HGNC:10971, MGC24091, MGC45202, NLT, OAT2Other
Designations: liver-specific transporter; organic anion transporter 2; solute
carrier family 22 member 7Chromosome: 6; Location: 6p21.2-p21.1GeneID: 10864
7: LOC442273 
similar to solute carrier family 22 member 3; organic cation transporter 3;
extraneuronal monoamine transporter; EMT organic cation transporter 3 [Homo
sapiens]Chromosome: 6; Location: 6q26GeneID: 442273
8: SLC22A2 
solute carrier family 22 (organic cation transporter), member 2 [Homo
sapiens]Other Aliases: HGNC:10966, OCT2Other Designations: organic cation
transporter 2; solute carrier family 22 member 2Chromosome: 6; Location:
6q26GeneID: 6582
9: SLC22A1 
solute carrier family 22 (organic cation transporter), member 1 [Homo
sapiens]Other Aliases: HGNC:10963, HOCT1, OCT1Other Designations: organic cation
transporter 1; solute carrier family 22 member 1Chromosome: 6; Location:
6q26GeneID: 6580
10: SLC17A2 
solute carrier family 17 (sodium phosphate), member 2 [Homo sapiens]Other
Aliases: HGNC:10930, NPT3Other Designations: sodium phosphate transporter 3;
solute carrier family 17 (vesicular glutamate transporter), member 2Chromosome:
6; Location: 6p21.3GeneID: 10246
11: SLC17A1 
solute carrier family 17 (sodium phosphate), member 1 [Homo sapiens]Other
Aliases: HGNC:10929, NAPI-1, NPT1Other Designations: solute carrier family 17
(vesicular glutamate transporter), member 1Chromosome: 6; Location:
6p23-p21.3GeneID: 6568
12: SLC39A7 
solute carrier family 39 (zinc transporter), member 7 [Homo sapiens]Other
Aliases: HGNC:4927, D6S115E, D6S2244E, H2-KE4, HKE4, KE4, RING5Other
Designations: HLA class II region expressed gene KE4; Ke4 gene, mouse, human
homolog ofChromosome: 6; Location: 6p21.3GeneID: 7922
13: SLC2A12 
solute carrier family 2 (facilitated glucose transporter), member 12 [Homo
sapiens]Other Aliases: HGNC:18067, GLUT12, GLUT8Chromosome: 6; Location:
6q23.2GeneID: 154091
14: SLC17A5 
solute carrier family 17 (anion/sugar transporter), member 5 [Homo sapiens]Other
Aliases: HGNC:10933, AST, ISSD, NSD, SD, SIALIN, SIASD, SLDOther Designations:
sialic acid storage disease; solute carrier family 17, member 5Chromosome: 6;
Location: 6q14-q15GeneID: 26503
15: C6orf85 
chromosome 6 open reading frame 85 [Homo sapiens]Other Aliases: HGNC:21106,
DKFZP434F011, FLJ22174Other Designations: ion transporter proteinChromosome: 6;
Location: 6p25.2GeneID: 63027
16: SLC16A10 
solute carrier family 16 (monocarboxylic acid transporters), member 10 [Homo
sapiens]Other Aliases: HGNC:17027, PRO0813, TAT1Other Designations: T-type amino
acid transporter 1; solute carrier family 16, member 10Chromosome: 6; Location:
6q21-q22GeneID: 117247
17: SLC26A8 
solute carrier family 26, member 8 [Homo sapiens]Other Aliases: HGNC:14468,
TAT1Other Designations: anion transporter/exchanger-8; testis anion transporter
1Chromosome: 6; Location: 6p21GeneID: 116369
18: KIF13A 
kinesin family member 13A [Homo sapiens]Other Aliases: HGNC:14566,
bA500C11.2Other Designations: homolog of mouse KIF13A mannose-6-phosphate
receptor transporterChromosome: 6; Location: 6p23GeneID: 63971
19: SLC35B2 
solute carrier family 35, member B2 [Homo sapiens]Other Aliases: HGNC:16872,
PAPST1, UGTrel4Other Designations: 3'-phosphoadenosine 5'-phosphosulfate
transporterChromosome: 6; Location: 6p12.1-p11.2GeneID: 347734
20: FABP7 
fatty acid binding protein 7, brain [Homo sapiens]Other Aliases: HGNC:3562,
B-FABP, FABPB, MRGOther Designations: mammary-derived growth
inhibitor-relatedChromosome: 6; Location: 6q22-q23GeneID: 2173
21: C6orf192 
chromosome 6 open reading frame 192 [Homo sapiens]Other Aliases: HGNC:21573,
dJ55C23.6Other Designations: dJ55C23.6 geneChromosome: 6; Location:
6q22.3-q23.3GeneID: 116843
22: RHAG 
Rhesus blood group-associated glycoprotein [Homo sapiens]Other Aliases:
HGNC:10006, RH2, RH50AChromosome: 6; Location: 6p21.1-p11GeneID: 6005
23: SLC29A1 
solute carrier family 29 (nucleoside transporters), member 1 [Homo sapiens]Other
Aliases: HGNC:11003, ENT1Chromosome: 6; Location: 6p21.1-p21.2GeneID: 2030
24: IBRDC2 
IBR domain containing 2 [Homo sapiens]Other Aliases: HGNC:21578, MGC71786,
bA528A10.3, p53RFPOther Designations: p53-inducible RING finger
proteinChromosome: 6; Location: 6p22.3GeneID: 255488
25: MRS2L 
MRS2-like, magnesium homeostasis factor (S. cerevisiae) [Homo sapiens]Other
Aliases: HGNC:13785, HPT, MRS2Other Designations: MRS2 (S. cerevisiae)-like,
magnesium homeostasis factor; MRS2-like, magnesium homeostasis factorChromosome:
6; Location: 6p22.3-p22.1GeneID: 57380
26: APOM 
apolipoprotein M [Homo sapiens]Other Aliases: HGNC:13916, G3a, HSPC336,
MGC22400, NG20Other Designations: NG20-like proteinChromosome: 6; Location:
6p21.33GeneID: 55937
27: CLIC5 
chloride intracellular channel 5 [Homo sapiens]Other Aliases: HGNC:13517,
CLIC5BChromosome: 6; Location: 6p12.1-21.1GeneID: 53405
28: CYP39A1 
cytochrome P450, family 39, subfamily A, polypeptide 1 [Homo sapiens]Other
Aliases: HGNC:17449Other Designations: cytochrome P450, subfamily XXXIX
(oxysterol 7 alpha-hydroxylase), polypeptide 1; oxysterol
7alpha-hydroxylaseChromosome: 6; Location: 6p21.1-p11.2GeneID: 51302
29: DDO 
D-aspartate oxidase [Homo sapiens]Other Aliases: HGNC:2727, DASOX, DDO-1,
DDO-2Other Designations: aspartic oxidaseChromosome: 6; Location: 6q21GeneID:
8528
30: STX7 
syntaxin 7 [Homo sapiens]Other Aliases: HGNC:11442Chromosome: 6; Location:
6q23.1GeneID: 8417
31: NQO2 
NAD(P)H dehydrogenase, quinone 2 [Homo sapiens]Other Aliases: HGNC:7856, DHQV,
NMOR2, QR2Other Designations: NAD(P)H menadione oxidoreductase 2,
dioxin-inducible; NAD(P)H menadione oxidoreductase-1,
dioxin-inducible-2Chromosome: 6; Location: 6pter-q12GeneID: 4835
32: ME1 
malic enzyme 1, NADP(+)-dependent, cytosolic [Homo sapiens]Other Aliases:
HGNC:6983, HUMNDME, MESOther Designations: Malic enzyme, cytoplasmic;
NADP-dependent malic enzyme; cytosolic malic enzyme 1; malate dehydrogenase;
malic enzyme 1, soluble; pyruvic-malic carboxylaseChromosome: 6; Location:
6q12GeneID: 4199
33: IGF2R 
insulin-like growth factor 2 receptor [Homo sapiens]Other Aliases: HGNC:5467,
CD222, CIMPR, M6P-R, MPRIOther Designations: Insulin-like growth factor-2
receptor (mannose-6-phosphate receptor, cation-independent); cation-independent
mannose-6 phosphate receptorChromosome: 6; Location: 6q26GeneID: 3482
34: SLC17A3 
solute carrier family 17 (sodium phosphate), member 3 [Homo sapiens]Other
Aliases: HGNC:10931, NPT4Chromosome: 6; Location: 6p21.3GeneID: 10786
35: SLC25A27 
solute carrier family 25, member 27 [Homo sapiens]Other Aliases: HGNC:21065,
FLJ33552, UCP4Other Designations: uncoupling protein 4Chromosome: 6; Location:
6p11.2-q12GeneID: 9481
36: ALDH5A1 
aldehyde dehydrogenase 5 family, member A1 (succinate-semialdehyde
dehydrogenase) [Homo sapiens]Other Aliases: HGNC:408, SSADH, SSDHOther
Designations: NAD(+)-dependent succinic semialdehyde dehydrogenase; aldehyde
dehydrogenase 5A1; mitochondrial succinate semialdehyde dehydrogenaseChromosome:
6; Location: 6p22.2-p22.3GeneID: 7915
37: LPA 
lipoprotein, Lp(a) [Homo sapiens]Other Aliases: HGNC:6667, AK38, LPOther
Designations: Apolipoprotein Lp(a); antiangiogenic AK38 proteinChromosome: 6;
Location: 6q26-q27GeneID: 4018
38: KPNA5 
karyopherin alpha 5 (importin alpha 6) [Homo sapiens]Other Aliases: HGNC:6398,
IPOA6, SRP6Other Designations: importin alpha 6Chromosome: 6; Location:
6q22.1GeneID: 3841
39: THSD2 
thrombospondin, type I, domain containing 2 [Homo sapiens]Other Aliases:
HGNC:20866, FLJ14440, PWTSROther Designations: thrombospondin-like
geneChromosome: 6; Location: 6q22.33GeneID: 84870
40: TXNDC5 
thioredoxin domain containing 5 [Homo sapiens]Other Aliases: HGNC:21073, ERP46,
EndoPDI, MGC3178, UNQ364Other Designations: endothelial protein disulphide
isomerase; thioredoxin related proteinChromosome: 6; Location: 6p24.3GeneID:
81567
41: GOPC 
golgi associated PDZ and coiled-coil motif containing [Homo sapiens]Other
Aliases: HGNC:17643, CAL, FIG, GOPC1, PISTOther Designations: CFTR-associated
ligand; Golgi associated PDZ and coiled-coil motif containing protein;
PDZ/coiled-coil domain binding partner for the rho-family GTPase TC10; dJ94G16.2
PIST; fused in glioblastomaChromosome: 6; Location: 6q21GeneID: 57120
42: PIP3-E 
phosphoinositide-binding protein PIP3-E [Homo sapiens]Other Aliases: IPCEF1,
KIAA0403Other Designations: interaction protein for cytohesin exchange factors 1
Interaction protein for cytohesin exchange factors 1Chromosome: 6; Location:
6q25.2GeneID: 26034
43: TXNL2 
thioredoxin-like 2 [Homo sapiens]Other Aliases: HGNC:15987, PICOTOther
Designations: PKC-interacting cousin of thioredoxin; thioredoxin-likeChromosome:
6; Location: 6p25.3GeneID: 10539
44: SLC17A4 
solute carrier family 17 (sodium phosphate), member 4 [Homo sapiens]Other
Aliases: HGNC:10932, KAIA2138Other Designations: Na/PO4 cotransporterChromosome:
6; Location: 6p22-p21.3GeneID: 10050
45: NUP153 
nucleoporin 153kDa [Homo sapiens]Other Aliases: HGNC:8062, HNUP153, N153Other
Designations: nuclear pore complex protein hnup153Chromosome: 6; Location:
6p22.3GeneID: 9972
46: STX11 
syntaxin 11 [Homo sapiens]Other Aliases: HGNC:11429Chromosome: 6; Location:
6q24.2GeneID: 8676
47: GRIK2 
glutamate receptor, ionotropic, kainate 2 [Homo sapiens]Other Aliases:
HGNC:4580, EAA4, GLR6, GLUR6Other Designations: excitatory amino acid receptor
4; glutamate receptor 6Chromosome: 6; Location: 6q16.3-q21GeneID: 2898
48: GPX5 
glutathione peroxidase 5 (epididymal androgen-related protein) [Homo
sapiens]Other Aliases: HGNC:4557Other Designations: epididymal androgen-related
protein; glutathione peroxidase 5Chromosome: 6; Location: 6p22.1GeneID: 2880
49: 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
50: COX7A2 
cytochrome c oxidase subunit VIIa polypeptide 2 (liver) [Homo sapiens]Other
Aliases: HGNC:2288, COX7AL, COX7AL1, COXVIIa-LOther Designations: hepatic
cytochrome-c oxidase chain VIIaChromosome: 6; Location: 6q12GeneID: 1347
51: ATP6V1G2 
ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G isoform 2 [Homo
sapiens]Other Aliases: HGNC:862, ATP6G, ATP6G2, NG38, Vma10Other Designations:
ATPase, H+ transporting, lysosomal (vacuolar proton pump); ATPase, H+
transporting, lysosomal (vacuolar proton pump) subunit G isoform 2; ATPase, H+
transporting, lysosomal 13kD, V1 subunit G isoform 2; ATPase, H+ transporting,
lysosomal, V1 subunit G2; H(+)-transporting two-sector ATPase, subunit G2;
V-ATPase 13 kDa subunit 2; V-ATPase G subunit 2; vacuolar ATP synthase subunit G
2; vacuolar ATPase G synthetase subunit; vacuolar proton pump G subunit
2Chromosome: 6; Location: 6p21.3GeneID: 534
52: TAPBP 
TAP binding protein (tapasin) [Homo sapiens]Other Aliases: HGNC:11566, NGS17,
TAPA, TPN, TPSNOther Designations: TAP-associated protein; TAP-binding protein;
tapasinChromosome: 6; Location: 6p21.3GeneID: 6892
53: SGK 
serum/glucocorticoid regulated kinase [Homo sapiens]Other Aliases: HGNC:10810,
SGK1Other Designations: serine/threonine protein kinase SGKChromosome: 6;
Location: 6q23GeneID: 6446
54: ABCC10 
ATP-binding cassette, sub-family C (CFTR/MRP), member 10 [Homo sapiens]Other
Aliases: HGNC:52, EST182763, MRP7, SIMRP7Other Designations: ATP-binding
cassette, sub-family C, member 10; multidrug resistance-associated protein
7Chromosome: 6; Location: 6p21.1GeneID: 89845