1: SLC19A2 
solute carrier family 19 (thiamine transporter), member 2 [Homo sapiens]Other
Aliases: HGNC:10938, TC1, THT1, THTR1, TRMAOther Designations: high affinity
thiamine transporter; reduced folate carrier protein (RFC) like; solute carrier
family 19, member 2; thiamine carrier 1; thiamine transporter 1Chromosome: 1;
Location: 1q23.3GeneID: 10560
2: SLC1A7 
solute carrier family 1 (glutamate transporter), member 7 [Homo sapiens]Other
Aliases: HGNC:10945, AAAT, EAAT5Other Designations: excitatory amino acid
transporter 5 (retinal glutamate transporter)Chromosome: 1; Location:
1p32.3GeneID: 6512
3: SLC30A7 
solute carrier family 30 (zinc transporter), member 7 [Homo sapiens]Other
Aliases: HGNC:19306, ZNT7, ZnTL2Other Designations: zinc transporter ZnT-7; zinc
transporter like 2Chromosome: 1; Location: 1p21.2GeneID: 148867
4: SLC2A5 
solute carrier family 2 (facilitated glucose/fructose transporter), member 5
[Homo sapiens]Other Aliases: HGNC:11010, GLUT5Other Designations: solute carrier
family 2 (facilitated glucose transporter), member 5Chromosome: 1; Location:
1p36.2GeneID: 6518
5: SLC35A3 
solute carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter),
member A3 [Homo sapiens]Other Aliases: HGNC:11023Other Designations: solute
carrier family 35 (UDP-N-acetylglucosamine (UDP-GlcNAc) transporter), member
3Chromosome: 1; Location: 1p21GeneID: 23443
6: SLC30A10 
solute carrier family 30 (zinc transporter), member 10 [Homo sapiens]Other
Aliases: DKFZp547M236, ZNT8, ZnT-10Other Designations: zinc transporter
8Chromosome: 1; Location: 1q41GeneID: 55532
7: SLC30A1 
solute carrier family 30 (zinc transporter), member 1 [Homo sapiens]Other
Aliases: HGNC:11012, ZNT1Other Designations: zinc transporter 1Chromosome: 1;
Location: 1q32-q41GeneID: 7779
8: ABCA4 
ATP-binding cassette, sub-family A (ABC1), member 4 [Homo sapiens]Other Aliases:
HGNC:34, ABC10, ABCR, FFM, RMP, RP19, STGD, STGD1Other Designations: ATP binding
cassette transporter; ATP-binding cassette, sub-family A member 4; ATP-binding
transporter, retina-specific; rim proteinChromosome: 1; Location:
1p22.1-p21GeneID: 24
9: SLC39A1 
solute carrier family 39 (zinc transporter), member 1 [Homo sapiens]Other
Aliases: HGNC:12876, ZIP1, ZIRTLOther Designations: solute carrier family 39
(zinc transporter), member 3; zinc-iron regulated transporter-like gene;
zinc/iron regulated transporter-likeChromosome: 1; Location: 1q21GeneID: 27173
10: SLC22A15 
solute carrier family 22 (organic cation transporter), member 15 [Homo
sapiens]Other Aliases: HGNC:20301, DKFZp761G0313, FLIPT1Other Designations:
fly-like putative organic ion transporter 1Chromosome: 1; Location:
1p13.1GeneID: 55356
11: SLC35D1 
solute carrier family 35 (UDP-glucuronic acid/UDP-N-acetylgalactosamine dual
transporter), member D1 [Homo sapiens]Other Aliases: HGNC:20800, KIAA0260,
UGTREL7Other Designations: UDP-glucuronic acid/UDP-N-acetylgalactosamine dual
transporterChromosome: 1; Location: 1p32-p31GeneID: 23169
12: SLC30A2 
solute carrier family 30 (zinc transporter), member 2 [Homo sapiens]Other
Aliases: HGNC:11013, MGC11303, ZNT2, ZnT-2Other Designations: solute carrier
family 30, member 2; zinc transporter 2Chromosome: 1GeneID: 7780
13: LOC391045 
similar to Solute carrier family 2, facilitated glucose transporter, member 3
(Glucose transporter type 3, brain) [Homo sapiens]Chromosome: 1; Location:
1p31.3GeneID: 391045
14: SLC2A7 
solute carrier family 2 (facilitated glucose transporter), member 7 [Homo
sapiens]Other Aliases: HGNC:13445, GLUT7Other Designations: intestinal
facilitative glucose transporter 7Chromosome: 1GeneID: 155184
15: SLC25A24 
solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 24
[Homo sapiens]Other Aliases: HGNC:20662, APC1, DKFZp586G0123, SCAMC-1Other
Designations: calcium-binding transporter; mitochondrial ATP-Mg/Pi transporter;
short calcium-binding mitochondrial carrier 1; solute carrier family 25 member
24Chromosome: 1; Location: 1p13.3GeneID: 29957
16: LOC388657 
similar to solute carrier family 25 member 24 isoform 2; calcium-binding
transporter; mitochondrial ATP-Mg/Pi transporter; short calcium-binding
mitochondrial carrier 1 [Homo sapiens]Chromosome: 1; Location: 1p13.3GeneID:
388657
17: SLC2A1 
solute carrier family 2 (facilitated glucose transporter), member 1 [Homo
sapiens]Other Aliases: HGNC:11005, GLUT, GLUT1Chromosome: 1; Location:
1p35-p31.3GeneID: 6513
18: SLC16A1 
solute carrier family 16 (monocarboxylic acid transporters), member 1 [Homo
sapiens]Other Aliases: HGNC:10922, MCT, MCT1Other Designations: monocarboxylate
transporter 1; solute carrier family 16, member 1Chromosome: 1; Location:
1p12GeneID: 6566
19: SLC16A4 
solute carrier family 16 (monocarboxylic acid transporters), member 4 [Homo
sapiens]Other Aliases: HGNC:10925, MCT4Other Designations: monocarboxylate
transporter 4; solute carrier family 16, member 4Chromosome: 1; Location:
1p13.3GeneID: 9122
20: SLC6A9 
solute carrier family 6 (neurotransmitter transporter, glycine), member 9 [Homo
sapiens]Other Aliases: HGNC:11056, GLYT1Chromosome: 1; Location: 1p33GeneID:
6536
21: ARHGEF11 
Rho guanine nucleotide exchange factor (GEF) 11 [Homo sapiens]Other Aliases:
HGNC:14580, GTRAP48, KIAA0380, PDZ-RHOGEFOther Designations: Rho guanine
exchange factor (GEF) 11; RhoA-specific guanine nucleotide exchange factor;
RhoGEF glutamate transport modulator; glutamate transporter EAAT4-associated
protein 48Chromosome: 1; Location: 1q21GeneID: 9826
22: LOC400785 
similar to putative UST1-like organic anion transporter [Homo
sapiens]Chromosome: 1; Location: 1q21.3GeneID: 400785
23: SLC6A17 
solute carrier family 6 (neurotransmitter transporter), member 17 [Homo
sapiens]Other Aliases: HGNC:31399Chromosome: 1; Location: 1p13.3GeneID: 388662
24: SLC27A3 
solute carrier family 27 (fatty acid transporter), member 3 [Homo sapiens]Other
Aliases: HGNC:10997, FATP3, MGC4365Other Designations: fatty acid transport
protein 3; solute carrier family 27 member 3Chromosome: 1; Location:
1q21.3GeneID: 11000
25: SLC2A3P2 
solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 2
[Homo sapiens]Other Aliases: HGNC:31074Chromosome: 1; Location: 1p31.3GeneID:
399493
26: NUP133 
nucleoporin 133kDa [Homo sapiens]Other Aliases: HGNC:18016, FLJ10814, MGC21133,
hNUP133Chromosome: 1; Location: 1q42.13GeneID: 55746
27: R-spondin 
likely ortholog of mouse roof plate-specific spondin [Homo sapiens]Other
Aliases: FLJ40906Other Designations: hypothetical protein FLJ40906Chromosome: 1;
Location: 1p34.3GeneID: 284654
28: LOC127262 
hypothetical protein LOC127262 [Homo sapiens]Chromosome: 1; Location:
1p36.32GeneID: 127262
29: ATP6V1G3 
ATPase, H+ transporting, lysosomal 13kDa, V1 subunit G isoform 3 [Homo
sapiens]Other Aliases: HGNC:18265, ATP6G3, Vma10Other Designations: ATPase, H+
transporting, lysosomal (vacuolar proton pump) subunit G3; ATPase, H+
transporting, lysosomal 13kD, V1 subunit G isoform 3; ATPase, H+ transporting,
lysosomal, V1 subunit G3; V-ATPase 13 kDa subunit 3; V-ATPase G subunit 3;
V-ATPase G3 subunit; vacuolar ATP synthase subunit G 3; vacuolar proton pump G
subunit 3; vacuolar proton pump, subunit G3Chromosome: 1; Location:
1q31.3GeneID: 127124
30: FLVCR 
feline leukemia virus subgroup C cellular receptor [Homo sapiens]Other
Designations: FLVCR proteinChromosome: 1; Location: 1q32.3GeneID: 28982
31: KPNA6 
karyopherin alpha 6 (importin alpha 7) [Homo sapiens]Other Aliases: HGNC:6399,
FLJ11249, IPOA7, KPNA7, MGC17918Other Designations: importin alpha 7 subunit;
importin-alpha-S2; karyopherin alpha 6Chromosome: 1; Location:
1p35.1-p34.3GeneID: 23633
32: ABCB10 
ATP-binding cassette, sub-family B (MDR/TAP), member 10 [Homo sapiens]Other
Aliases: HGNC:41, EST20237, M-ABC2, MTABC2Other Designations: ATP-binding
cassette, sub-family B, member 10Chromosome: 1; Location: 1q42GeneID: 23456
33: COG2 
component of oligomeric golgi complex 2 [Homo sapiens]Other Aliases: HGNC:6546,
LDLCOther Designations: brefeldin A-sensitive, peripheral Golgi protein;
conserved oligomeric Golgi complex protein 2; low density lipoprotein receptor
defect C complementingChromosome: 1; Location: 1q42.2GeneID: 22796
34: CFHL4 
complement factor H-related 4 [Homo sapiens]Other Aliases: HGNC:16979, FHR-4,
FHR4Chromosome: 1; Location: 1q32GeneID: 10877
35: CLCA3 
chloride channel, calcium activated, family member 3 [Homo sapiens]Other
Aliases: HGNC:2017Other Designations: calcium activated chloride channel
3Chromosome: 1; Location: 1p31-p22GeneID: 9629
36: H6PD 
hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase) [Homo sapiens]Other
Aliases: HGNC:4795, G6PDH, GDHOther Designations: GDH/6PGL endoplasmic
bifunctional protein; glucose dehydrogenase; hexose-6-phosphate
dehydrogenaseChromosome: 1; Location: 1p36GeneID: 9563
37: KMO 
kynurenine 3-monooxygenase (kynurenine 3-hydroxylase) [Homo sapiens]Other
Aliases: HGNC:6381Chromosome: 1; Location: 1q42-q44GeneID: 8564
38: SORT1 
sortilin 1 [Homo sapiens]Other Aliases: HGNC:11186, Gp95, NT3Other Designations:
neurotensin receptor 3Chromosome: 1; Location: 1p21.3-p13.1GeneID: 6272
39: QSCN6 
quiescin Q6 [Homo sapiens]Other Aliases: HGNC:9756, Q6, QSOX1Chromosome: 1;
Location: 1q24GeneID: 5768
40: PPOX 
protoporphyrinogen oxidase [Homo sapiens]Other Aliases: HGNC:9280, MGC8485, PPO,
VPChromosome: 1; Location: 1q22GeneID: 5498
41: PLOD 
procollagen-lysine, 2-oxoglutarate 5-dioxygenase (lysine hydroxylase,
Ehlers-Danlos syndrome type VI) [Homo sapiens]Other Aliases: HGNC:9081, LH, LLH,
PLOD1Other Designations: lysine hydroxylase; lysyl hydroxylaseChromosome: 1;
Location: 1p36.3-p36.2GeneID: 5351
42: PDZK1 
PDZ domain containing 1 [Homo sapiens]Other Aliases: HGNC:8821, CAP70, CLAMP,
PDZD1Chromosome: 1; Location: 1q21GeneID: 5174
43: PDC 
phosducin [Homo sapiens]Other Aliases: HGNC:8759, MEKA, PHD, PhLOP, PhLPOther
Designations: 33kDA phototransducing protein; G beta gamma binding protein; MEKA
protein; phosducin-like orphan protein; phosducin-like proteinChromosome: 1;
Location: 1q25.2GeneID: 5132
44: NCF2 
neutrophil cytosolic factor 2 (65kDa, chronic granulomatous disease, autosomal
2) [Homo sapiens]Other Aliases: HGNC:7661, NOXA2, P67-PHOX, p67phoxOther
Designations: neutrophil cytosolic factor 2; neutrophil cytosolic factor 2
(65kD, chronic granulomatous disease, autosomal 2)Chromosome: 1; Location:
1q25GeneID: 4688
45: LAMB3 
laminin, beta 3 [Homo sapiens]Other Aliases: HGNC:6490, LAMNB1Other
Designations: BM600-125kDa; kalinin-140kDa; laminin subunit beta 3; laminin,
beta 3 (nicein (125kD), kalinin (140kD), BM600 (125kD));
nicein-125kDaChromosome: 1; Location: 1q32GeneID: 3914
46: CRABP2 
cellular retinoic acid binding protein 2 [Homo sapiens]Other Aliases: HGNC:2339,
CRABP-II, RBP6Other Designations: cellular retinoic acid-binding protein
2Chromosome: 1; Location: 1q21.3GeneID: 1382
47: ATP6V0B 
ATPase, H+ transporting, lysosomal 21kDa, V0 subunit c'' [Homo sapiens]Other
Aliases: HGNC:861, ATP6F, HATPL, VMA16Other Designations: ATPase, H+
transporting, lysosomal (vacuolar proton pump) 21kD; H(+)-transporting
two-sector ATPase, subunit F; vacuolar ATP synthase 21 kDa proteolipid subunit;
vacuolar proton pump, 21 kDa subunitChromosome: 1; Location: 1p32.3GeneID: 533
48: ATP5F1 
ATP synthase, H+ transporting, mitochondrial F0 complex, subunit b, isoform 1
[Homo sapiens]Other Aliases: HGNC:840, MGC24431Other Designations: ATP synthase
B chain, mitochondrial; ATP synthase, H+ transporting, mitochondrial F0 complex,
subunit b; H+-ATP synthase subunit bChromosome: 1; Location: 1p13.2GeneID: 515
49: ATP1A1 
ATPase, Na+/K+ transporting, alpha 1 polypeptide [Homo sapiens]Other Aliases:
HGNC:799, MGC3285, MGC51750Other Designations: Na+/K+ -ATPase alpha 1 subunit;
Na+/K+ ATPase 1; Na, K-ATPase, alpha-A catalytic polypeptide; sodium pump 1;
sodium-potassium-ATPase, alpha 1 polypeptideChromosome: 1; Location: 1p21GeneID:
476
50: SYT14 
synaptotagmin XIV [Homo sapiens]Other Aliases: HGNC:23143, FLJ34198,
sytXIVChromosome: 1; Location: 1q32.2GeneID: 255928
51: SLC41A1 
solute carrier family 41, member 1 [Homo sapiens]Other Aliases: HGNC:19429,
MgtEOther Designations: solute carrier family 41 member 1Chromosome: 1;
Location: 1q32.1GeneID: 254428
52: RBP7 
retinol binding protein 7, cellular [Homo sapiens]Other Aliases: HGNC:30316,
CRBP4, CRBPIVOther Designations: putative cellular retinol-binding protein CRBP
IV; retinoid binding protein 7Chromosome: 1; Location: 1p36.22GeneID: 116362
53: AQP10 
aquaporin 10 [Homo sapiens]Other Aliases: HGNC:16029, AQPA_HUMANOther
Designations: small intestine aquaporinChromosome: 1; Location: 1q21.3GeneID:
89872
54: DISP1 
dispatched homolog 1 (Drosophila) [Homo sapiens]Other Aliases: HGNC:19711,
DISPA, DKFZP434I0428, MGC13130, MGC16796Other Designations: dispatched
AChromosome: 1; Location: 1q41GeneID: 84976
55: SYTL1 
synaptotagmin-like 1 [Homo sapiens]Other Aliases: HGNC:15584, FLJ14996, JFC1,
SLP1Other Designations: NADPH oxidase-related, C2 domain-containing
proteinChromosome: 1; Location: 1p36.11GeneID: 84958
56: HIAT1 
hippocampus abundant transcript 1 [Homo sapiens]Other Aliases: HGNC:23363,
DKFZP564L0864Other Designations: hippocampus abundant gene transcript 1;
tetracycline transporter-like proteinChromosome: 1; Location: 1p21.3GeneID:
64645
57: RHBG 
Rhesus blood group, B glycoprotein [Homo sapiens]Other Aliases: HGNC:14572Other
Designations: Rh type B glycoproteinChromosome: 1; Location: 1q21.3GeneID: 57127
58: PHGDH 
phosphoglycerate dehydrogenase [Homo sapiens]Other Aliases: HGNC:8923, 3PGDH,
MGC3017, PDG, PGAD, PGD, PGDH, SERAOther Designations: 3-phosphoglycerate
dehydrogenaseChromosome: 1; Location: 1p12GeneID: 26227
59: KIAA0962 
KIAA0962 protein [Homo sapiens]Chromosome: 1; Location: 1p36.1GeneID: 23341
60: VPS45A 
vacuolar protein sorting 45A (yeast) [Homo sapiens]Other Aliases: HGNC:14579,
H1, H1VPS45, VPS45, VPS45B, VPS54A, VSP45, VSP45AOther Designations: leucocyte
vacuolar protein sorting 45; vacuolar protein sorting 45A; vacuolar protein
sorting 45B (yeast)Chromosome: 1; Location: 1q21-q22GeneID: 11311
61: AP4B1 
adaptor-related protein complex 4, beta 1 subunit [Homo sapiens]Other Aliases:
HGNC:572, BETA-4Other Designations: beta 4 subunit of AP-4Chromosome: 1;
Location: 1p13.2GeneID: 10717
62: AKR1A1 
aldo-keto reductase family 1, member A1 (aldehyde reductase) [Homo sapiens]Other
Aliases: HGNC:380, ALDR1, ALR, MGC12529, MGC1380Other Designations: alcohol
dehydrogenase; aldehyde reductase; aldo-keto reductase family 1, member
A1Chromosome: 1; Location: 1p33-p32GeneID: 10327
63: KIAA0446 
KIAA0446 gene product [Homo sapiens]Chromosome: 1; Location: 1q22GeneID: 9673
64: IPO13 
importin 13 [Homo sapiens]Other Aliases: HGNC:16853, IMP13, KAP13, KIAA0724,
RANBP13Other Designations: Ran binding protein 13; karyopherin 13Chromosome: 1;
Location: 1p34.1GeneID: 9670
65: ALDH4A1 
aldehyde dehydrogenase 4 family, member A1 [Homo sapiens]Other Aliases:
HGNC:406, ALDH4, P5CD, P5CDh, P5CDhL, P5CDhSOther Designations: P5C
dehydrogenase; aldehyde dehydrogenase 4A1; mitochondrial delta-1-pyrroline
5-carboxylate dehydrogenaseChromosome: 1; Location: 1p36GeneID: 8659
66: DEGS 
degenerative spermatocyte homolog, lipid desaturase (Drosophila) [Homo
sapiens]Other Aliases: HGNC:13709, DES1, Des-1, MGC5079, MLDOther Designations:
degenerative spermatocyte (homolog Drosophila; lipid desaturase);
dihydroceramide desaturase; membrane fatty acid (lipid) desaturase; sphingolipid
delta 4 desaturaseChromosome: 1; Location: 1q42.12GeneID: 8560
67: STXBP3 
syntaxin binding protein 3 [Homo sapiens]Other Aliases: HGNC:11446, MUNC18-3,
MUNC18C, PSP, UNC-18COther Designations: syntaxin 4 binding proteinChromosome:
1; Location: 1p13.3GeneID: 6814
68: SDHC 
succinate dehydrogenase complex, subunit C, integral membrane protein, 15kDa
[Homo sapiens]Other Aliases: HGNC:10682, PGL3, SDH3Other Designations:
paraganglioma or familial glomus tumors 3; succinate dehydrogenase complex,
subunit C; succinate-ubiquinone oxidoreducatase cytochrome B large
subunitChromosome: 1; Location: 1q21GeneID: 6391
69: PIGR 
polymeric immunoglobulin receptor [Homo sapiens]Other Aliases: HGNC:8968Other
Designations: hepatocellular carcinoma associated protein TB6Chromosome: 1;
Location: 1q31-q41GeneID: 5284
70: GRIK3 
glutamate receptor, ionotropic, kainate 3 [Homo sapiens]Other Aliases:
HGNC:4581, EAA5, GLR7, GLUR7Other Designations: excitatory amino acid receptor
5; glutamate receptor 7Chromosome: 1; Location: 1p34-p33GeneID: 2899
71: FABP3 
fatty acid binding protein 3, muscle and heart (mammary-derived growth
inhibitor) [Homo sapiens]Other Aliases: HGNC:3557, FABP11, H-FABP, MDGI,
O-FABPOther Designations: Fatty acid-binding protein 3, muscle; fatty acid
binding protein 11; fatty acid binding protein 3; mammary-derived growth
inhibitorChromosome: 1; Location: 1p33-p32GeneID: 2170
72: ALDH9A1 
aldehyde dehydrogenase 9 family, member A1 [Homo sapiens]Other Aliases:
HGNC:412, ALDH4, ALDH7, ALDH9, E3, TMABADHOther Designations:
4-trimethylaminobutyraldehyde dehydrogenase; R-aminobutyraldehyde dehydrogenase;
aldehyde dehydrogenase (NAD+); aldehyde dehydrogenase 9A1; aldehyde
dehydrogenase E3 isozyme; gamma-aminobutyraldehyde dehydrogenaseChromosome: 1;
Location: 1q23.1GeneID: 223
73: SYT6 
synaptotagmin VI [Homo sapiens]Other Aliases: HGNC:18638Chromosome: 1; Location:
1p13.2GeneID: 148281
74: SYT2 
synaptotagmin II [Homo sapiens]Other Aliases: HGNC:11510, SytIIOther
Designations: synaptotagmin 2Chromosome: 1; Location: 1q32.1GeneID: 127833
75: TLP19 
endoplasmic reticulum thioredoxin superfamily member, 18 kDa [Homo sapiens]Other
Aliases: ERP18, ERP19Other Designations: thioredoxin-like protein p19Chromosome:
1; Location: 1p32.3GeneID: 51060
76: SYT11 
synaptotagmin XI [Homo sapiens]Other Aliases: HGNC:19239, KIAA0080, MGC10881,
MGC17226, SYT12Other Designations: synaptotagmin 12Chromosome: 1; Location:
1q21.2GeneID: 23208
77: AKR7A3 
aldo-keto reductase family 7, member A3 (aflatoxin aldehyde reductase) [Homo
sapiens]Other Aliases: HGNC:390, AFAR2Other Designations: aflatoxin B1 aldehyde
reductase 2; aldo-keto reductase family 7, member A3Chromosome: 1; Location:
1p35.1-p36.23GeneID: 22977
78: ZFYVE9 
zinc finger, FYVE domain containing 9 [Homo sapiens]Other Aliases: HGNC:6775,
MADHIP, NSP, SARA, SMADIPOther Designations: MAD homolog interacting protein;
MAD, mothers against decapentaplegic homolog (Drosophila) interacting protein,
receptor activation anchor; MADH-interacting protein; mothers against
decapentaplegic homolog (Drosophila) interacting protein; novel serine protease;
receptor activation anchor; smad anchor for receptor activationChromosome: 1;
Location: 1p32.3GeneID: 9372
79: DHRS3 
dehydrogenase/reductase (SDR family) member 3 [Homo sapiens]Other Aliases:
HGNC:17693, Rsdr1, SDR1, retSDR1Other Designations: short-chain
dehydrogenase/reductase 1Chromosome: 1; Location: 1p36.1GeneID: 9249
80: AKR7A2 
aldo-keto reductase family 7, member A2 (aflatoxin aldehyde reductase) [Homo
sapiens]Other Aliases: HGNC:389, AFAR, AFAR1, AFB1-AR1, AKR7Other Designations:
aflatoxin beta1 aldehyde reductase; aldo-keto reductase family 7, member A2;
aldoketoreductase 7Chromosome: 1; Location: 1p35.1-p36.23GeneID: 8574
81: TSNAX 
translin-associated factor X [Homo sapiens]Other Aliases: HGNC:12380, TRAXOther
Designations: translin-like proteinChromosome: 1; Location: 1q42.1GeneID: 7257
82: SDHB 
succinate dehydrogenase complex, subunit B, iron sulfur (Ip) [Homo sapiens]Other
Aliases: HGNC:10681, IP, SDH, SDH1, SDHIPOther Designations: iron-sulfur
subunitChromosome: 1; Location: 1p36.1-p35GeneID: 6390
83: PGD 
phosphogluconate dehydrogenase [Homo sapiens]Other Aliases: HGNC:8891, 6PGDOther
Designations: 6-phosphogluconate dehydrogenaseChromosome: 1; Location:
1p36.3-p36.13GeneID: 5226
84: GJA8 
gap junction protein, alpha 8, 50kDa (connexin 50) [Homo sapiens]Other Aliases:
HGNC:4281, CAE, CAE1, CX50, CZP1, MP70Other Designations: Gap junction membrane
channel protein alpha-8 (connexin 50); connexin 50; gap junction membrane
channel protein alpha-8; gap junction protein, alpha 8, 50kD (connexin
50)Chromosome: 1; Location: 1q21.1GeneID: 2703
85: DPYD 
dihydropyrimidine dehydrogenase [Homo sapiens]Other Aliases: HGNC:3012, DHP,
DPDChromosome: 1; Location: 1p22GeneID: 1806
86: COPA 
coatomer protein complex, subunit alpha [Homo sapiens]Other Aliases: HGNC:2230,
HEP-COPOther Designations: alpha coat protein; xeninChromosome: 1; Location:
1q23-q25GeneID: 1314
87: ATP1A4 
ATPase, Na+/K+ transporting, alpha 4 polypeptide [Homo sapiens]Other Aliases:
HGNC:14073, ATP1AL2, MGC25056Other Designations: ATPase, Na+/K+ transporting,
alpha polypeptide-like 2; Na+/K+ -ATPase alpha 4 subunit; Na+/K+ ATPase 4;
Na+/K+ ATPase, alpha-D polypeptide; sodium pump 4; sodium/potassium-transporting
ATPase alpha-4 chainChromosome: 1; Location: 1q21-q23GeneID: 480
88: ATP1A2 
ATPase, Na+/K+ transporting, alpha 2 (+) polypeptide [Homo sapiens]Other
Aliases: HGNC:800, FHM2, MGC59864, MHP2Other Designations: Na+/K+ -ATPase alpha
2 subunit proprotein; Na+/K+ ATPase 2; Na+/K+ ATPase, alpha-A(+) catalytic
polypeptide; Na+/K+ ATPase, alpha-B polypeptide; migraine, hemiplegic 2; sodium
pump 2; sodium-potassium ATPase; sodium/potassium-transporting ATPase alpha-2
chainChromosome: 1; Location: 1q21-q23GeneID: 477
89: APOA2 
apolipoprotein A-II [Homo sapiens]Other Aliases: HGNC:601Chromosome: 1;
Location: 1q21-q23GeneID: 336
90: ABCD3 
ATP-binding cassette, sub-family D (ALD), member 3 [Homo sapiens]Other Aliases:
HGNC:67, ABC43, PMP70, PXMP1Other Designations: ATP-binding cassette, sub-family
D, member 3; Peroxisomal membrane protein-1 (70kD); peroxisomal membrane protein
1 (70kD, Zellweger syndrome); peroxisomal membrane protein-1Chromosome: 1;
Location: 1p22-p21GeneID: 5825
91: SLC26A9 
solute carrier family 26, member 9 [Homo sapiens]Other Aliases: HGNC:14469Other
Designations: anion transporter/exchanger-9Chromosome: 1; Location:
1q31-q32GeneID: 115019
92: RSC1A1 
regulatory solute carrier protein, family 1, member 1 [Homo sapiens]Other
Aliases: HGNC:10458, RS1Chromosome: 1; Location: 1p36.1GeneID: 6248
93: RHCE 
Rhesus blood group, CcEe antigens [Homo sapiens]Other Aliases: HGNC:10008, RH,
RH30A, RHC, RHE, RHIXB, RHPI, Rh4, RhVI, RhVIIIOther Designations: Rh blood
group C antigen; Rh blood group antigen Evans; Rh polypeptide I; Rhesus system C
and E polypeptides; membrane protein RhCeChromosome: 1; Location: 1p36.11GeneID:
6006