1: SLC6A4 
solute carrier family 6 (neurotransmitter transporter, serotonin), member 4
[Homo sapiens]Other Aliases: HGNC:11050, 5-HTT, SERTOther Designations:
5-hydroxytryptamine transporter; 5HT transporter; Na+/Cl- dependent serotonin
transporter; sodium-dependent serotonin transporter; solute carrier family 6
member 4Chromosome: 17; Location: 17q11.1-q12GeneID: 6532
2: SLC13A5 
solute carrier family 13 (sodium-dependent citrate transporter), member 5 [Homo
sapiens]Other Aliases: HGNC:23089, NACTOther Designations: sodium-coupled
citrate transporterChromosome: 17; Location: 17p13.1GeneID: 284111
3: SLC2A4 
solute carrier family 2 (facilitated glucose transporter), member 4 [Homo
sapiens]Other Aliases: HGNC:11009, GLUT4Chromosome: 17; Location: 17p13GeneID:
6517
4: ABCC3 
ATP-binding cassette, sub-family C (CFTR/MRP), member 3 [Homo sapiens]Other
Aliases: HGNC:54, ABC31, EST90757, MLP2, MOAT-D, MRP3, cMOAT2Other Designations:
ATP-binding cassette, sub-family C, member 3; canicular multispecific organic
anion transporterChromosome: 17; Location: 17q22GeneID: 8714
5: SLC16A6 
solute carrier family 16 (monocarboxylic acid transporters), member 6 [Homo
sapiens]Other Aliases: HGNC:10927, MCT6Other Designations: monocarboxylate
transporter 6; solute carrier family 16, member 6Chromosome: 17; Location:
17q24.2GeneID: 9120
6: SLC13A2 
solute carrier family 13 (sodium-dependent dicarboxylate transporter), member 2
[Homo sapiens]Other Aliases: HGNC:10917, NADC1, NaDC-1Chromosome: 17; Location:
17p13.2GeneID: 9058
7: SLC39A11 
solute carrier family 39 (metal ion transporter), member 11 [Homo sapiens]Other
Aliases: HGNC:14463, C17orf26Other Designations: chromosome 17 open reading
frame 26Chromosome: 17; Location: 17q24.3-q25.1GeneID: 201266
8: SLC25A10 
solute carrier family 25 (mitochondrial carrier; dicarboxylate transporter),
member 10 [Homo sapiens]Other Aliases: HGNC:10980, DICOther Designations:
dicarboxylate ion carrierChromosome: 17; Location: 17q25.3GeneID: 1468
9: SLC35B1 
solute carrier family 35, member B1 [Homo sapiens]Other Aliases: HGNC:20798,
UGTREL1Other Designations: UDP-galactose transporter relatedChromosome: 17;
Location: 17q21.33GeneID: 10237
10: SLC16A5 
solute carrier family 16 (monocarboxylic acid transporters), member 5 [Homo
sapiens]Other Aliases: HGNC:10926, MCT5Other Designations: monocarboxylate
transporter 5; solute carrier family 16, member 5Chromosome: 17; Location:
17q25.1GeneID: 9121
11: SLC16A3 
solute carrier family 16 (monocarboxylic acid transporters), member 3 [Homo
sapiens]Other Aliases: HGNC:10924, MCT3, MCT4Other Designations: monocarboxylate
transporter 3; solute carrier family 16, member 3Chromosome: 17; Location:
17q25GeneID: 9123
12: SLC16A13 
solute carrier family 16 (monocarboxylic acid transporters), member 13 [Homo
sapiens]Other Aliases: HGNC:31037Other Designations: monocarboxylate transporter
13Chromosome: 17; Location: 17p13.1GeneID: 201232
13: LOC440459 
similar to solute carrier family 16, member 6; monocarboxylate transporter 6
[Homo sapiens]Chromosome: 17GeneID: 440459
14: ABCA6 
ATP-binding cassette, sub-family A (ABC1), member 6 [Homo sapiens]Other Aliases:
HGNC:36, EST155051Other Designations: ABC transporter ABCA6; ATP-binding
cassette A6; ATP-binding cassette, sub-family A, member 6Chromosome: 17;
Location: 17q24.3GeneID: 23460
15: SLC25A19 
solute carrier family 25 (mitochondrial deoxynucleotide carrier), member 19
[Homo sapiens]Other Aliases: HGNC:14409, DNC, MCPHA, MUP1Other Designations:
deoxynucleotide carrier, mitochondrial; mitochondrial uncoupling protein
1Chromosome: 17; Location: 17q25.3GeneID: 60386
16: PITPNA 
phosphatidylinositol transfer protein, alpha [Homo sapiens]Other Aliases:
HGNC:9001, PITPN, VIB1AOther Designations: phosphotidylinositol transfer
proteinChromosome: 17; Location: 17p13.3GeneID: 5306
17: G6PC 
glucose-6-phosphatase, catalytic (glycogen storage disease type I, von Gierke
disease) [Homo sapiens]Other Aliases: HGNC:4056, G6PT, GSD1aOther Designations:
Glucose-6-phosphatase, catalytic; glucose-6-phosphatase, catalyticChromosome:
17; Location: 17q21GeneID: 2538
18: MGC29671 
hypothetical protein MGC29671 [Homo sapiens]Chromosome: 17; Location:
17p13.2GeneID: 201305
19: SLC16A11 
solute carrier family 16 (monocarboxylic acid transporters), member 11 [Homo
sapiens]Other Aliases: HGNC:23093, FLJ90193Other Designations: solute carrier
family 16, member 11Chromosome: 17; Location: 17p13.1GeneID: 162515
20: LOC124976 
hypothetical protein LOC124976 [Homo sapiens]Chromosome: 17; Location:
17p13.2GeneID: 124976
21: MGC15523 
hypothetical protein MGC15523 [Homo sapiens]Chromosome: 17; Location:
17q25.3GeneID: 124565
22: FLJ10847 
hypothetical protein FLJ10847 [Homo sapiens]Chromosome: 17; Location:
17p11.2GeneID: 55244
23: PITPNC1 
phosphatidylinositol transfer protein, cytoplasmic 1 [Homo sapiens]Other
Aliases: HGNC:21045, RDGB-BETA, RDGBB, RDGBB1Other Designations: retinal
degeneration B beta 1 (Drosophila)Chromosome: 17; Location: 17q24.2GeneID: 26207
24: TOM1L1 
target of myb1-like 1 (chicken) [Homo sapiens]Other Aliases: HGNC:11983,
SRCASMOther Designations: Src activating and signaling molecule; target of myb
1-like 1; target of myb1 (chicken) homolog-like 1; target of myb1-like
1Chromosome: 17; Location: 17q23.2GeneID: 10040
25: TRIP3 
thyroid hormone receptor interactor 3 [Homo sapiens]Other Aliases: HGNC:12309,
ZNHIT3Other Designations: thyroid receptor interacting protein 3; zinc finger,
HIT domain containing 3Chromosome: 17; Location: 17q12GeneID: 9326
26: AOC3 
amine oxidase, copper containing 3 (vascular adhesion protein 1) [Homo
sapiens]Other Aliases: HGNC:550, HPAO, VAP-1, VAP1Other Designations: amine
oxidase (copper-containing);copper amine oxidase precursor ;vascular adhesion
protein 1; copper containing amine oxidase 3; vascular adhesion protein
1Chromosome: 17; Location: 17q21GeneID: 8639
27: DOC2B 
double C2-like domains, beta [Homo sapiens]Other Aliases: HGNC:2986Chromosome:
17; Location: 17p13.3GeneID: 8447
28: SLC25A11 
solute carrier family 25 (mitochondrial carrier; oxoglutarate carrier), member
11 [Homo sapiens]Other Aliases: HGNC:10981, OGC, SLC20A4Other Designations:
solute carrier family 20 (oxoglutarate carrier), member 4Chromosome: 17;
Location: 17p13.3GeneID: 8402
29: EPX 
eosinophil peroxidase [Homo sapiens]Other Aliases: HGNC:3423, EPO, EPP,
EPX-PENChromosome: 17; Location: 17q23.1GeneID: 8288
30: SLC4A1 
solute carrier family 4, anion exchanger, member 1 (erythrocyte membrane protein
band 3, Diego blood group) [Homo sapiens]Other Aliases: HGNC:11027, AE1, BND3,
CD233, DI, EMPB3, EPB3, RTA1A, WD, WD1Other Designations: Waldner blood group;
anion exchange protein 1Chromosome: 17; Location: 17q21-q22GeneID: 6521
31: FALZ 
fetal Alzheimer antigen [Homo sapiens]Other Aliases: HGNC:3581, BPTF, FAC1,
NURF301Other Designations: bromodomain and PHD domain transcription factor;
fetal Alz-50 reactive clone 1; nucleosome remodeling factor, large
subunitChromosome: 17; Location: 17q24.3GeneID: 2186
32: CHRNE 
cholinergic receptor, nicotinic, epsilon polypeptide [Homo sapiens]Other
Aliases: HGNC:1966, ACHREOther Designations: nicotinic acetylcholine receptor
epsilon polypeptideChromosome: 17; Location: 17p13-p12GeneID: 1145
33: APOH 
apolipoprotein H (beta-2-glycoprotein I) [Homo sapiens]Other Aliases: HGNC:616,
B2G1, BGOther Designations: beta-2-glycoprotein IChromosome: 17; Location:
17q23-qterGeneID: 350
34: AOC2 
amine oxidase, copper containing 2 (retina-specific) [Homo sapiens]Other
Aliases: HGNC:549, DAO2, RAOOther Designations: Amine oxidase,
copper-containing, 2; copper containing 2 (retina-specific); copper containing
amine oxidaseChromosome: 17; Location: 17q21GeneID: 314
35: ALOX12B 
arachidonate 12-lipoxygenase, 12R type [Homo sapiens]Other Aliases: HGNC:430,
12R-LOXChromosome: 17; Location: 17p13.1GeneID: 242
36: 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
37: SLC5A10 
solute carrier family 5 (sodium/glucose cotransporter), member 10 [Homo
sapiens]Other Aliases: HGNC:23155, FLJ25217, SGLT5Chromosome: 17; Location:
17p11.2GeneID: 125206
38: CYGB 
cytoglobin [Homo sapiens]Other Aliases: HGNC:16505, HGB, STAPOther Designations:
histoglobin; stellate cell activation-associated proteinChromosome: 17;
Location: 17q25.3GeneID: 114757
39: TXNL5 
thioredoxin-like 5 [Homo sapiens]Other Aliases: HGNC:28218, MGC14353, TRP14Other
Designations: thioredoxin (Trx)-related protein, 14 kDaChromosome: 17; Location:
17p13.1GeneID: 84817
40: FLJ20255 
hypothetical protein FLJ20255 [Homo sapiens]Chromosome: 17; Location:
17q25.1GeneID: 54868
41: CACNG5 
calcium channel, voltage-dependent, gamma subunit 5 [Homo sapiens]Other Aliases:
HGNC:1409Other Designations: neuronal voltage-gated calcium channel gamma-5
subunit; voltage-dependent calcium channel gamma-5 subunitChromosome: 17;
Location: 17q24GeneID: 27091
42: STARD3 
START domain containing 3 [Homo sapiens]Other Aliases: HGNC:17579, CAB1, MLN64,
es64Other Designations: steroidogenic acute regulatory protein
relatedChromosome: 17; Location: 17q11-q12GeneID: 10948
43: CCT6B 
chaperonin containing TCP1, subunit 6B (zeta 2) [Homo sapiens]Other Aliases:
HGNC:1621, CCTZ-2, Cctz2, TSA303Chromosome: 17; Location: 17q12GeneID: 10693
44: COG1 
component of oligomeric golgi complex 1 [Homo sapiens]Other Aliases: HGNC:6545,
DKFZP762L1710, KIAA1381, LDLBOther Designations: conserved oligomeric Golgi
complex protein 1; low density lipoprotein B; low density lipoprotein receptor
defect B complementingChromosome: 17; Location: 17q25.1GeneID: 9382
45: SEC14L1 
SEC14-like 1 (S. cerevisiae) [Homo sapiens]Other Aliases: HGNC:10698,
SEC14LOther Designations: SEC14 (S. cerevisiae)-like 1Chromosome: 17; Location:
17q25.1-17q25.2GeneID: 6397
46: NUP88 
nucleoporin 88kDa [Homo sapiens]Other Aliases: HGNC:8067, MGC8530Other
Designations: karyoporin; nuclear pore complex protein 88Chromosome: 17;
Location: 17p13.2GeneID: 4927
47: 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
48: KPNA2 
karyopherin alpha 2 (RAG cohort 1, importin alpha 1) [Homo sapiens]Other
Aliases: HGNC:6395, IPOA1, QIP2, RCH1, SRP1alphaOther Designations: RAG cohort
1; importin alpha 1; importin alpha 2; importin-alpha-P1; karyopherin alpha 2;
pendulinChromosome: 17; Location: 17q23.1-q23.3GeneID: 3838
49: ATP6V0A1 
ATPase, H+ transporting, lysosomal V0 subunit a isoform 1 [Homo sapiens]Other
Aliases: HGNC:865, ATP6N1, ATP6N1A, Stv1, VPP1, Vph1, a1Other Designations:
ATPase, H+ transporting, lysosomal (vacuolar proton pump) non-catalytic
accessory protein 1A (110/116kD); ATPase, H+ transporting, lysosomal
non-catalytic accessory protein 1 (110/116kD); H(+)-transporting two-sector
ATPase, 116 kDa accessory protein A1; clathrin-coated vesicle/synaptic vesicle
proton pump 116 kDa subunit; vacuolar proton pump, subunit 1; vacuolar proton
translocating ATPase 116 kDa subunit A isoform 1; vacuolar-type H(+)-ATPase 115
kDa subunitChromosome: 17; Location: 17q21GeneID: 535
50: ALOX15B 
arachidonate 15-lipoxygenase, second type [Homo sapiens]Other Aliases:
HGNC:434Chromosome: 17; Location: 17p13.1GeneID: 247
51: FLJ31196 
hypothetical protein FLJ31196 [Homo sapiens]Chromosome: 17; Location:
17p11.2GeneID: 146802
52: TOM1L2 
target of myb1-like 2 (chicken) [Homo sapiens]Other Aliases: HGNC:11984,
FLJ32746Other Designations: target of myb1 (chicken) homolog-like 1; target of
myb1 (chicken) homolog-like 2; target of myb1-like 2Chromosome: 17; Location:
17p11.2GeneID: 146691
53: MGC9564 
similar to RIKEN cDNA 1110002C08 gene [Homo sapiens]Other Designations:
hypothetical protein MGC9564Chromosome: 17; Location: 17q11.2GeneID: 113235
54: PITPNM3 
PITPNM family member 3 [Homo sapiens]Other Aliases: HGNC:21043, NIR1,
RDGBA3Other Designations: PYK2 N-terminal domain-interacting receptor 1; retinal
degeneration B alpha 3 (Drosophila)Chromosome: 17; Location: 17p13GeneID: 83394
55: NXN 
nucleoredoxin [Homo sapiens]Other Aliases: HGNC:18008, FLJ12614Other
Designations: nucleoredoxin 1Chromosome: 17; Location: 17p13.3GeneID: 64359
56: PCTP 
phosphatidylcholine transfer protein [Homo sapiens]Other Aliases: HGNC:8752,
STARD2Other Designations: START domain containing 2Chromosome: 17; Location:
17q21-q24GeneID: 58488
57: TRPV2 
transient receptor potential cation channel, subfamily V, member 2 [Homo
sapiens]Other Aliases: HGNC:18082, MGC12549, VRL, VRL-1, VRL1Other Designations:
vanilloid receptor-like protein 1Chromosome: 17; Location: 17p11.2GeneID: 51393
58: TIMM22 
translocase of inner mitochondrial membrane 22 homolog (yeast) [Homo
sapiens]Other Aliases: HGNC:17317, TEX4, TIM22Other Designations: putative
membrane protein; testis-expressed sequence 4; translocase of inner
mitochondrial membrane 22 (yeast) homologChromosome: 17; Location: 17p13GeneID:
29928
59: NARF 
nuclear prelamin A recognition factor [Homo sapiens]Other Aliases:
DKFZp434G0420, FLJ10067Chromosome: 17; Location: 17q25.3GeneID: 26502
60: GGA3 
golgi associated, gamma adaptin ear containing, ARF binding protein 3 [Homo
sapiens]Other Aliases: HGNC:17079, KIAA0154Other Designations: ADP-ribosylation
factor binding protein 3; Golgi-localized, gamma ear-containing, ARF-binding
protein 3Chromosome: 17; Location: 17q25.1GeneID: 23163
61: RAMP2 
receptor (calcitonin) activity modifying protein 2 [Homo sapiens]Other Aliases:
HGNC:9844Other Designations: calcitonin receptor-like receptor activity
modifying protein 2; receptor-activity-modifying protein 2Chromosome: 17;
Location: 17q12-q21.1GeneID: 10266
62: GOSR2 
golgi SNAP receptor complex member 2 [Homo sapiens]Other Aliases: HGNC:4431,
GS27, MEMBRINChromosome: 17; Location: 17q21GeneID: 9570
63: P4HB 
procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), beta
polypeptide (protein disulfide isomerase; thyroid hormone binding protein p55)
[Homo sapiens]Other Aliases: HGNC:8548, DSI, ERBA2L, GIT, PDI, PO4DB, PO4HB,
PROHBOther Designations: disulfide isomerase; glutathione-insulin
transhydrogenase; prolyl 4-hydroxylase, beta subunit; protein disulfide
isomerase/oxidoreductase; thyroid hormone-binding protein p55; v-erb-a avian
erythroblastic leukemia viral oncogene homolog 2-likeChromosome: 17; Location:
17q25GeneID: 5034
64: KPNB1 
karyopherin (importin) beta 1 [Homo sapiens]Other Aliases: HGNC:6400, IMB1,
IPOB, Impnb, MGC2155, MGC2156, MGC2157, NTF97Other Designations: importin 90;
importin beta-1 subunit; karyopherin beta 1; nuclear factor p97Chromosome: 17;
Location: 17q21.32GeneID: 3837
65: CTNS 
cystinosis, nephropathic [Homo sapiens]Other Aliases: HGNC:2518, CTNS-LSBOther
Designations: CystinosisChromosome: 17; Location: 17p13GeneID: 1497
66: COX11 
COX11 homolog, cytochrome c oxidase assembly protein (yeast) [Homo sapiens]Other
Aliases: HGNC:2261, COX11POther Designations: COX11 (yeast) homolog, cytochrome
c oxidase assembly protein; COX11 homolog; cytochrome c oxidase assembly protein
COX11; cytochrome c oxidase subunit 11Chromosome: 17; Location: 17q22GeneID:
1353
67: CHRNB1 
cholinergic receptor, nicotinic, beta polypeptide 1 (muscle) [Homo sapiens]Other
Aliases: HGNC:1961, ACHRB, CHRNBOther Designations: nicotinic acetylcholine
receptor beta subunitChromosome: 17; Location: 17p13.1GeneID: 1140
68: ATP5G1 
ATP synthase, H+ transporting, mitochondrial F0 complex, subunit c (subunit 9),
isoform 1 [Homo sapiens]Other Aliases: HGNC:841, ATP5GOther Designations: ATP
synthase lipid-binding protein, mitochondrial; ATP synthase proteolipid P1; ATP
synthase, H+ transporting, mitochondrial F0 complex, subunit c, isoform 1;
ATPase protein 9; ATPase subunit C; mitochondrial ATP synthase, subunit C
(subunit 9), isoform 1Chromosome: 17; Location: 17q21.32GeneID: 516
69: MAP2K3 
mitogen-activated protein kinase kinase 3 [Homo sapiens]Other Aliases:
HGNC:6843, MAPKK3, MEK3, MKK3, PRKMK3Other Designations: MAP kinase kinase 3;
MAPK/ERK kinase 3; dual specificity mitogen activated protein kinase kinase
3Chromosome: 17; Location: 17q11.2GeneID: 5606
70: PRKWNK4 
protein kinase, lysine deficient 4 [Homo sapiens]Other Aliases: HGNC:14544,
PHA2B, WNK4Other Designations: putative protein kinase WNK4Chromosome: 17;
Location: 17q21-q22GeneID: 65266
71: PRKCA 
protein kinase C, alpha [Homo sapiens]Other Aliases: HGNC:9393, PKC-alpha, PKCA,
PRKACAOther Designations: protein kinase C, alpha polypeptideChromosome: 17;
Location: 17q22-q23.2GeneID: 5578