1: ASNA1 
arsA arsenite transporter, ATP-binding, homolog 1 (bacterial) [Homo
sapiens]Other Aliases: HGNC:752, ARSA-I, ARSA1, MGC3821Other Designations: arsA
(bacterial) arsenite transporter, ATP-binding, homolog 1; arsA arsenite
transporter, ATP-binding, homolog 1Chromosome: 19; Location: 19q13.3GeneID: 439
2: SLC7A10 
solute carrier family 7, (neutral amino acid transporter, y+ system) member 10
[Homo sapiens]Other Aliases: HGNC:11058, FLJ20839, HASC-1, asc-1Other
Designations: asc-type amino acid transporter 1; solute carrier family 7,
(cationic amino acid transporter, y+ system) member 10; solute carrier family 7,
member 10Chromosome: 19; Location: 19q13.1GeneID: 56301
3: SLC7A9 
solute carrier family 7 (cationic amino acid transporter, y+ system), member 9
[Homo sapiens]Other Aliases: HGNC:11067, CSNU3Other Designations: solute carrier
family 7 (cationic amino acid, transporter, y+ system), member 9; solute carrier
family 7, member 9Chromosome: 19; Location: 19q13.1GeneID: 11136
4: SLC39A3 
solute carrier family 39 (zinc transporter), member 3 [Homo sapiens]Other
Aliases: HGNC:17128, ZIP3Other Designations: zinc transporterChromosome: 19;
Location: 19p13.3GeneID: 29985
5: SLC1A5 
solute carrier family 1 (neutral amino acid transporter), member 5 [Homo
sapiens]Other Aliases: HGNC:10943, AAAT, ASCT2, ATBO, M7V1, M7VS1, R16,
RDRCOther Designations: RD114 virus receptor; baboon M7 virus receptor; neutral
amino acid transporter BChromosome: 19; Location: 19q13.3GeneID: 6510
6: SLC1A6 
solute carrier family 1 (high affinity aspartate/glutamate transporter), member
6 [Homo sapiens]Other Aliases: HGNC:10944, EAAT4Other Designations: excitatory
amino acid transporter 4Chromosome: 19; Location: 19p13.12GeneID: 6511
7: LOC284379 
similar to solute carrier family 7, member 3; amino acid transporter, cationic
3; solute carrier family 7 (cationic amino acid transporter, y+ system), member
3 [Homo sapiens]Chromosome: 19; Location: 19q13.42GeneID: 284379
8: SLC17A7 
solute carrier family 17 (sodium-dependent inorganic phosphate cotransporter),
member 7 [Homo sapiens]Other Aliases: HGNC:16704, BNPI, VGLUT1Other
Designations: brain-specific Na-dependent inorganic phosphate cotransporter;
solute carrier family 17, member 7; vesicular glutamate transporter 1Chromosome:
19; Location: 19q13GeneID: 57030
9: ABCA7 
ATP-binding cassette, sub-family A (ABC1), member 7 [Homo sapiens]Other Aliases:
HGNC:37, ABCA-SSN, ABCXOther Designations: ATP-binding cassette, sub-family A,
member 7; autoantigen SS-N; macrophage ABC transporterChromosome: 19; Location:
19p13.3GeneID: 10347
10: SLC6A16 
solute carrier family 6 (neurotransmitter transporter), member 16 [Homo
sapiens]Other Aliases: HGNC:13622, NTT5Other Designations: NTT5
proteinChromosome: 19; Location: 19q13.1-q13.4GeneID: 28968
11: SLC27A1 
solute carrier family 27 (fatty acid transporter), member 1 [Homo sapiens]Other
Aliases: HGNC:10995, FATP, FATP1, FLJ00336, MGC71751Chromosome: 19; Location:
19p13.11GeneID: 376497
12: SLC27A5 
solute carrier family 27 (fatty acid transporter), member 5 [Homo sapiens]Other
Aliases: HGNC:10999, FACVL3, FATP5, FLJ22987, VLACSR, VLCS-H2, VLCSH2Other
Designations: very long-chain acyl-CoA synthetase homolog 2; very long-chain
acyl-CoA synthetase-related proteinChromosome: 19; Location: 19q13.43GeneID:
10998
13: FCGRT 
Fc fragment of IgG, receptor, transporter, alpha [Homo sapiens]Other Aliases:
HGNC:3621, FCRNChromosome: 19; Location: 19q13.3GeneID: 2217
14: SLC5A5 
solute carrier family 5 (sodium iodide symporter), member 5 [Homo sapiens]Other
Aliases: HGNC:11040, NISChromosome: 19; Location: 19p13.2-p12GeneID: 6528
15: GRIN3B 
glutamate receptor, ionotropic, N-methyl-D-aspartate 3B [Homo sapiens]Other
Aliases: HGNC:16768, NR3BOther Designations: NMDA type glutamate receptor
subunit NR3B precursorChromosome: 19; Location: 19p13.3GeneID: 116444
16: SLC25A23 
solute carrier family 25 (mitochondrial carrier; phosphate carrier), member 23
[Homo sapiens]Other Aliases: HGNC:19375, APC2, MGC2615, SCaMC-3Other
Designations: short calcium-binding mitochondrial carrier 3Chromosome: 19;
Location: 19p13.3GeneID: 79085
17: DHX34 
DEAH (Asp-Glu-Ala-His) box polypeptide 34 [Homo sapiens]Other Aliases:
HGNC:16719, DDX34, HRH1, KIAA0134Other Designations: DEAD/H
(Asp-Glu-Ala-Asp/His) box polypeptide 34; probable ATP-dependent helicase
DHX34Chromosome: 19; Location: 19q13.3GeneID: 9704
18: PRDX2 
peroxiredoxin 2 [Homo sapiens]Other Aliases: HGNC:9353, MGC4104, NKEFB, PRP,
PRXII, TDPX1, TSAOther Designations: natural killer-enhancing factor B;
thiol-specific antioxidant 1; thioredoxin peroxidase 1; thioredoxin-dependent
peroxide reductase 1; torinChromosome: 19; Location: 19p13.2GeneID: 7001
19: GRIN2D 
glutamate receptor, ionotropic, N-methyl D-aspartate 2D [Homo sapiens]Other
Aliases: HGNC:4588, EB11, NMDAR2DOther Designations: N-methyl-D-aspartate
receptor subunit 2D; estrogen receptor binding CpG islandChromosome: 19;
Location: 19q13.1-qterGeneID: 2906
20: GPX4 
glutathione peroxidase 4 (phospholipid hydroperoxidase) [Homo sapiens]Other
Aliases: HGNC:4556, snGPxOther Designations: glutathione peroxidase 4;
phospholipid hydroperoxidase; sperm nucleus glutathione peroxidaseChromosome:
19; Location: 19p13.3GeneID: 2879
21: COX7A1 
cytochrome c oxidase subunit VIIa polypeptide 1 (muscle) [Homo sapiens]Other
Aliases: HGNC:2287, COX7A, COX7AH, COX7AMOther Designations: cytochrome c
oxidase subunit VIIa heart/muscle isoformChromosome: 19; Location:
19q13.1GeneID: 1346
22: AP2S1 
adaptor-related protein complex 2, sigma 1 subunit [Homo sapiens]Other Aliases:
HGNC:565, AP17, AP17-DELTA, CLAPS2Other Designations: AP17, delta variant;
clathrin assembly protein 2 small chain; clathrin-associated/assembly/adaptor
protein, small 2 (17kD)Chromosome: 19; Location: 19q13.2-q13.3GeneID: 1175
23: APOC2 
apolipoprotein C-II [Homo sapiens]Other Aliases: HGNC:609Chromosome: 19;
Location: 19q13.2GeneID: 344
24: APOC1 
apolipoprotein C-I [Homo sapiens]Other Aliases: HGNC:607Chromosome: 19;
Location: 19q13.2GeneID: 341
25: TXNL6 
thioredoxin-like 6 [Homo sapiens]Other Aliases: HGNC:25179, RDCVFOther
Designations: rod-derived cone viability factorChromosome: 19; Location:
19p13.11GeneID: 115861
26: UQCR 
ubiquinol-cytochrome c reductase (6.4kD) subunit [Homo sapiens]Chromosome: 19;
Location: 19p13.3GeneID: 10975
27: LDLR 
low density lipoprotein receptor (familial hypercholesterolemia) [Homo
sapiens]Other Aliases: HGNC:6547, FH, FHCOther Designations: LDL receptor; LDLR
precursor; low density lipoprotein receptorChromosome: 19; Location:
19p13.3GeneID: 3949
28: ATP1A3 
ATPase, Na+/K+ transporting, alpha 3 polypeptide [Homo sapiens]Other Aliases:
HGNC:801, MGC13276Other Designations: Na+/K+ -ATPase alpha 3 subunit; Na+/K+
ATPase 3; alpha(III); sodium pump 3; sodium-potassium-ATPase, alpha 3
polypeptide; sodium/potassium-transporting ATPase alpha-3 chainChromosome: 19;
Location: 19q13.31GeneID: 478
29: APOC4 
apolipoprotein C-IV [Homo sapiens]Other Aliases: HGNC:611Chromosome: 19;
Location: 19q13.2GeneID: 346
30: MGC19604 
similar to RIKEN cDNA B230118G17 gene [Homo sapiens]Other Designations:
hypothetical protein MGC19604; similar to P0671D01.19Chromosome: 19; Location:
19p13.2GeneID: 112812
31: SYT3 
synaptotagmin III [Homo sapiens]Other Aliases: HGNC:11511, DKFZp761O132,
SytIIIOther Designations: synaptotagmin 3Chromosome: 19; Location:
19q13.33GeneID: 84258
32: TTYH1 
tweety homolog 1 (Drosophila) [Homo sapiens]Other Aliases: HGNC:13476Other
Designations: tweety 1Chromosome: 19; Location: 19q13.4GeneID: 57348
33: TNPO2 
transportin 2 (importin 3, karyopherin beta 2b) [Homo sapiens]Other Aliases:
HGNC:19998, FLJ12155, IPO3, KPNB2B, TRN2Other Designations: importin 3;
karyopherin beta 2b, transportinChromosome: 19; Location: 19p13.13GeneID: 30000
34: DHDH 
dihydrodiol dehydrogenase (dimeric) [Homo sapiens]Other Aliases: HGNC:17887,
HUM2DDOther Designations: 3-deoxyglucosone reductase; dimeric dihydrodiol
dehydrogenaseChromosome: 19; Location: 19q13.3GeneID: 27294
35: COPE 
coatomer protein complex, subunit epsilon [Homo sapiens]Other Aliases:
HGNC:2234, FLJ13241, epsilon-COPOther Designations: coatomer epsilon subunit;
epsilon coat protein; epsilon subunit of coatomer protein complexChromosome: 19;
Location: 19p13.11GeneID: 11316
36: AP3D1 
adaptor-related protein complex 3, delta 1 subunit [Homo sapiens]Other Aliases:
HGNC:568, ADTDOther Designations: adaptin, deltaChromosome: 19; Location:
19p13.3GeneID: 8943
37: NAPA 
N-ethylmaleimide-sensitive factor attachment protein, alpha [Homo sapiens]Other
Aliases: HGNC:7641, SNAPAOther Designations: alpha-SNAPChromosome: 19; Location:
19q13.32GeneID: 8775
38: SYT5 
synaptotagmin V [Homo sapiens]Other Aliases: HGNC:11513Other Designations:
synaptotagmin 5Chromosome: 19; Location: 11pGeneID: 6861
39: STXBP2 
syntaxin binding protein 2 [Homo sapiens]Other Aliases: HGNC:11445, Hunc18b,
MUNC18-2, UNC18-2, UNC18BChromosome: 19; Location: 19p13.3-p13.2GeneID: 6813
40: GRIK5 
glutamate receptor, ionotropic, kainate 5 [Homo sapiens]Other Aliases:
HGNC:4583, EAA2, GRIK2, KA2Other Designations: excitatory amino acid receptor 2;
glutamate receptor KA2Chromosome: 19; Location: 19q13.2GeneID: 2901
41: ATP5D 
ATP synthase, H+ transporting, mitochondrial F1 complex, delta subunit [Homo
sapiens]Other Aliases: HGNC:837Other Designations: mitochondrial ATP synthase,
delta subunitChromosome: 19; Location: 19p13.3GeneID: 513
42: APOE 
apolipoprotein E [Homo sapiens]Other Aliases: HGNC:613, AD2, MGC1571Other
Designations: Alzheimer disease 2 (APOE*E4-associated, late onset);
apolipoprotein E precursor; apolipoprotein E3Chromosome: 19; Location:
19q13.2GeneID: 348