1: SLC6A19 
solute carrier family 6 (neurotransmitter transporter), member 19 [Homo
sapiens]Other Aliases: HGNC:27960, HNDOther Designations: amino acid transporter
system B0; sodium-dependent amino acid transporter; system B0 neutral amino acid
transporterChromosome: 5; Location: 5p15.33GeneID: 340024
2: SLC30A5 
solute carrier family 30 (zinc transporter), member 5 [Homo sapiens]Other
Aliases: HGNC:19089, FLJ12496, FLJ12756, MGC5499, ZNT5, ZNTL1, ZTL1, ZnT-5Other
Designations: zinc transporter 5; zinc transporter ZTL1Chromosome: 5; Location:
5q12.1GeneID: 64924
3: SLC22A5 
solute carrier family 22 (organic cation transporter), member 5 [Homo
sapiens]Other Aliases: HGNC:10969, OCTN2Other Designations: high-affinity sodium
dependent carnitine cotransporter; organic cation transporter 5; organic
cation/carnitine transporter 2; solute carrier family 22 member 5Chromosome: 5;
Location: 5q31GeneID: 6584
4: SLCO6A1 
solute carrier organic anion transporter family, member 6A1 [Homo sapiens]Other
Aliases: HGNC:23613, GST, MGC26949, OATP6A1, OATPYOther Designations:
gonad-specific transporter; testis-specific organic anion transporterChromosome:
5; Location: 5q21.1GeneID: 133482
5: SLC36A1 
solute carrier family 36 (proton/amino acid symporter), member 1 [Homo
sapiens]Other Aliases: HGNC:18761, LYAAT1, PAT1Other Designations: lysosomal
amino acid transporter 1; proton-coupled amino acid transporter; proton/amino
acid transporter 1; solute carrier family 36 member 1Chromosome: 5; Location:
5q33.1GeneID: 206358
6: SLC26A2 
solute carrier family 26 (sulfate transporter), member 2 [Homo sapiens]Other
Aliases: HGNC:10994, D5S1708, DTD, DTDST, EDM4, MST153, MSTP157Other
Designations: diastrophic dysplasia sulfate transporter; solute carrier family
26 member 2; sulfate anion transporter 1Chromosome: 5; Location: 5q31-q34GeneID:
1836
7: SLC6A3 
solute carrier family 6 (neurotransmitter transporter, dopamine), member 3 [Homo
sapiens]Other Aliases: HGNC:11049, DAT, DAT1Other Designations: dopamine
transporterChromosome: 5; Location: 5p15.3GeneID: 6531
8: SLC25A2 
solute carrier family 25 (mitochondrial carrier; ornithine transporter) member 2
[Homo sapiens]Other Aliases: HGNC:22921, ORNT2Other Designations: ornithine
transporter 2; solute carrier family 25 member 2Chromosome: 5; Location:
5q31GeneID: 83884
9: SLC22A4 
solute carrier family 22 (organic cation transporter), member 4 [Homo
sapiens]Other Aliases: HGNC:10968, MGC34546, OCTN1Other Designations: integral
membrane transport protein; organic cation transporter 4; solute carrier family
22 member 4Chromosome: 5; Location: 5q23.3GeneID: 6583
10: SLC6A7 
solute carrier family 6 (neurotransmitter transporter, L-proline), member 7
[Homo sapiens]Other Aliases: HGNC:11054, PROTOther Designations: brain-specific
L-proline transporter; solute carrier family 6, member 7Chromosome: 5; Location:
5q31-q32GeneID: 6534
11: SLC23A1 
solute carrier family 23 (nucleobase transporters), member 1 [Homo sapiens]Other
Aliases: HGNC:10974, MGC22361, SLC23A2, SVCT1, YSPL3Other Designations:
Na(+)/L-ascorbic acid transporter 1; sodium-dependent vitamin C transporter-1;
solute carrier family 23 (nucleobase transporters), member 2; yolk sac
permease-like molecule 3Chromosome: 5; Location: 5q31.2-q31.3GeneID: 9963
12: SLC1A3 
solute carrier family 1 (glial high affinity glutamate transporter), member 3
[Homo sapiens]Other Aliases: HGNC:10941, EAAT1, GLAST, GLAST1Chromosome: 5;
Location: 5p13GeneID: 6507
13: SLC12A7 
solute carrier family 12 (potassium/chloride transporters), member 7 [Homo
sapiens]Other Aliases: HGNC:10915, DKFZP434F076, KCC4Other Designations:
potassium/chloride transporter KCC4Chromosome: 5; Location: 5p15GeneID: 10723
14: SLC36A2 
solute carrier family 36 (proton/amino acid symporter), member 2 [Homo
sapiens]Other Aliases: HGNC:18762, PAT2, TRAMD1Other Designations: proton/amino
acid transporter 2; tramdorinChromosome: 5; Location: 5q33.1GeneID: 153201
15: MATP 
membrane associated transporter [Homo sapiens]Other Aliases: HGNC:16472, 1A1,
AIM1Other Designations: melanoma antigen AIM1; underwhiteChromosome: 5;
Location: 5p13.3GeneID: 51151
16: SLCO4C1 
solute carrier organic anion transporter family, member 4C1 [Homo sapiens]Other
Aliases: HGNC:23612, OATP-H, OATP-M1, OATP4C1, OATPX, PRO2176,
SLC21A20Chromosome: 5; Location: 5q21.2GeneID: 353189
17: SLC6A18 
solute carrier family 6 (neurotransmitter transporter), member 18 [Homo
sapiens]Other Aliases: HGNC:26441, FLJ31236, Xtrp2Chromosome: 5; Location:
5p15.33GeneID: 348932
18: SLC27A6 
solute carrier family 27 (fatty acid transporter), member 6 [Homo sapiens]Other
Aliases: HGNC:11000, FACVL2, FATP6, VLCS-H1Other Designations: very long-chain
acyl-CoA synthetase homolog 1Chromosome: 5; Location: 5q23.3GeneID: 28965
19: SLC36A3 
solute carrier family 36 (proton/amino acid symporter), member 3 [Homo
sapiens]Other Aliases: HGNC:19659, PAT3, TRAMD2, tramdorin2Other Designations:
proton/amino acid transporter 3; tramdorin 2Chromosome: 5; Location:
5q33.1GeneID: 285641
20: SLC35A4 
solute carrier family 35, member A4 [Homo sapiens]Other Aliases: HGNC:20753,
MGC2541Other Designations: solute carrier family 35 (UDP-galactose transporter),
member A4Chromosome: 5; Location: 5q31.3GeneID: 113829
21: SLC2A3P1 
solute carrier family 2 (facilitated glucose transporter), member 3 pseudogene 1
[Homo sapiens]Other Aliases: HGNC:11008, GLUT3P1, GLUT6, SLC2A3PChromosome: 5;
Location: 5q33-q35GeneID: 6516
22: NUP155 
nucleoporin 155kDa [Homo sapiens]Other Aliases: HGNC:8063, KIAA0791, N155Other
Designations: nuclear pore complex protein Nup155Chromosome: 5; Location:
5p13.1GeneID: 9631
23: ANKH 
ankylosis, progressive homolog (mouse) [Homo sapiens]Other Aliases: HGNC:15492,
ANK, CCAL2, CMDJ, CPPDD, HANK, MANKOther Designations: ankylosis, progressive
homologChromosome: 5; Location: 5p15.1GeneID: 56172
24: SLC12A2 
solute carrier family 12 (sodium/potassium/chloride transporters), member 2
[Homo sapiens]Other Aliases: HGNC:10911, BSC, BSC2, NKCC1Other Designations:
basolateral Na-K-Cl symporter; bumetanide-sensitive sodium-(potassium)-chloride
cotransporter 1Chromosome: 5; Location: 5q23.3GeneID: 6558
25: STARD4 
START domain containing 4, sterol regulated [Homo sapiens]Other Aliases:
HGNC:18058Other Designations: START domain containing 4
sterol-regulatedChromosome: 5; Location: 5q22.1GeneID: 134429
26: RANBP17 
RAN binding protein 17 [Homo sapiens]Other Aliases: HGNC:14428Chromosome: 5;
Location: 5q34GeneID: 64901
27: KIF20A 
kinesin family member 20A [Homo sapiens]Other Aliases: HGNC:9787, RAB6KIFLOther
Designations: RAB6 interacting, kinesin-like (rabkinesin6)Chromosome: 5;
Location: 5q31GeneID: 10112
28: SLC34A1 
solute carrier family 34 (sodium phosphate), member 1 [Homo sapiens]Other
Aliases: HGNC:11019, NAPI-3, NPT2, NPTIIa, SLC11, SLC17A2Other Designations:
sodium/phosphate co-transporter; solute carrier family 17 (sodium phosphate),
member 2Chromosome: 5; Location: 5q35GeneID: 6569
29: PAM 
peptidylglycine alpha-amidating monooxygenase [Homo sapiens]Other Aliases:
HGNC:8596, PAL, PHMOther Designations: pancreatic peptidylglycine
alpha-amidating monooxygenase; peptidyl alpha-amidating enzyme;
peptidyl-alpha-hydroxyglycine alpha-amidating lyase; peptidylglycine
2-hydroxylase; peptidylglycine alpha-hydroxylating monooxygenaseChromosome: 5;
Location: 5q14-q21GeneID: 5066
30: TNPO1 
transportin 1 [Homo sapiens]Other Aliases: HGNC:6401, IPO2, KPNB2, MIP, MIP1,
TRNOther Designations: M9 region interaction protein; importin beta 2;
karyopherin (importin) beta 2Chromosome: 5; Location: 5q13.2GeneID: 3842
31: SFXN1 
sideroflexin 1 [Homo sapiens]Other Aliases: HGNC:16085, FLJ12876Other
Designations: tricarboxylate carrier proteinChromosome: 5GeneID: 94081
32: NNT 
nicotinamide nucleotide transhydrogenase [Homo sapiens]Other Aliases:
HGNC:7863Chromosome: 5; Location: 5p13.1-5cenGeneID: 23530
33: RNF14 
ring finger protein 14 [Homo sapiens]Other Aliases: HGNC:10058, ARA54, HFB30,
HRIHFB2038Other Designations: androgen receptor associated protein 54; triad2
proteinChromosome: 5; Location: 5q23.3-q31.1GeneID: 9604
34: ATP6V0E 
ATPase, H+ transporting, lysosomal 9kDa, V0 subunit e [Homo sapiens]Other
Aliases: HGNC:863, ATP6H, M9.2, Vma21, Vma21pOther Designations: ATPase, H+
transporting, lysosomal (vacuolar proton pump) 9kD; ATPase, H+ transporting,
lysosomal 9kD V0 subunit M9.2; ATPase, H+ transporting, lysosomal 9kD V0 subunit
e; ATPase, H+ transporting, lysosomal, 9kD; ATPase, H+ transporting, lysosomal,
V0 subunit e; H(+)-transporting two-sector ATPase, subunit H; V-ATPase 9.2 kDa
membrane accessory protein; V-ATPase H subunit; V-ATPase M9.2 subunit; vacuolar
ATP synthase subunit H; vacuolar proton pump H subunit; vacuolar proton-ATPase
subunit M9.2Chromosome: 5; Location: 5q35.1GeneID: 8992
35: P4HA2 
procollagen-proline, 2-oxoglutarate 4-dioxygenase (proline 4-hydroxylase), alpha
polypeptide II [Homo sapiens]Other Aliases: HGNC:8547Other Designations: prolyl
4-hydroxylase, alpha polypeptide, type 2; prolyl-4-hydroxylase, alpha
polypeptide, type IIChromosome: 5; Location: 5q31GeneID: 8974
36: TCOF1 
Treacher Collins-Franceschetti syndrome 1 [Homo sapiens]Other Aliases:
HGNC:11654, MFD1, treacleOther Designations: Treacher Collins-Franceschetti
syndrome protein 1; treacleChromosome: 5; Location: 5q32-q33.1GeneID: 6949
37: SRD5A1 
steroid-5-alpha-reductase, alpha polypeptide 1 (3-oxo-5 alpha-steroid delta
4-dehydrogenase alpha 1) [Homo sapiens]Other Aliases: HGNC:11284Other
Designations: 3-oxo-5 alpha-steroid delta 4-dehydrogenase alpha 1; 5-alpha
reductase; steroid-5-alpha-reductase 1Chromosome: 5; Location: 5p15GeneID: 6715
38: SNX2 
sorting nexin 2 [Homo sapiens]Other Aliases: HGNC:11173, MGC5204Chromosome: 5;
Location: 5q23GeneID: 6643
39: HSD17B4 
hydroxysteroid (17-beta) dehydrogenase 4 [Homo sapiens]Other Aliases:
HGNC:5213Chromosome: 5; Location: 5q21GeneID: 3295
40: GRIA1 
glutamate receptor, ionotropic, AMPA 1 [Homo sapiens]Other Aliases: HGNC:4571,
GLUH1, GLUR1, GLURA, HBGR1Other Designations: AMPA 1Chromosome: 5; Location:
5q31.1GeneID: 2890
41: GPX3 
glutathione peroxidase 3 (plasma) [Homo sapiens]Other Aliases: HGNC:4555Other
Designations: plasma glutathione peroxidase 3Chromosome: 5; Location:
5q23GeneID: 2878
42: CDO1 
cysteine dioxygenase, type I [Homo sapiens]Other Aliases: HGNC:1795Chromosome:
5; Location: 5q22-q23GeneID: 1036
43: ATOX1 
ATX1 antioxidant protein 1 homolog (yeast) [Homo sapiens]Other Aliases:
HGNC:798, ATX1, HAH1Other Designations: ATX1 (antioxidant protein 1, yeast)
homolog 1; antioxidant protein 1; copper transport protein; metal transport
proteinChromosome: 5; Location: 5q32GeneID: 475
44: FLJ90709 
hypothetical protein FLJ90709 [Homo sapiens]Chromosome: 5; Location:
5q11.2GeneID: 153129
45: C5orf14 
chromosome 5 open reading frame 14 [Homo sapiens]Other Aliases: HGNC:20652,
FLJ22625, UNQ335Other Designations: 2310047H23Rik; disulfide
isomeraseChromosome: 5; Location: 5q31.1GeneID: 79770
46: G3BP 
Ras-GTPase-activating protein SH3-domain-binding protein [Homo sapiens]Other
Aliases: HDH-VIIIOther Designations: GAP binding protein; RasGAP-associated
endoribonuclease G3BPChromosome: 5; Location: 5q33.1GeneID: 10146
47: GLRX 
glutaredoxin (thioltransferase) [Homo sapiens]Other Aliases: HGNC:4330,
GRXChromosome: 5; Location: 5q14GeneID: 2745
48: FABP6 
fatty acid binding protein 6, ileal (gastrotropin) [Homo sapiens]Other Aliases:
HGNC:3561, I-15P, I-BABP, I-BAP, ILBP, ILBP3, ILLBPOther Designations:
gastrotropin; illeal lipid-binding proteinChromosome: 5; Location:
5q33.3-q34GeneID: 2172
49: AP3S1 
adaptor-related protein complex 3, sigma 1 subunit [Homo sapiens]Other Aliases:
HGNC:2013, CLAPS3, Sigma3AOther Designations:
clathrin-associated/assembly/adaptor protein, small 3 (22kD);
clathrin-associated/assembly/adaptor protein, small 3, 22-kD; Sigma3AChromosome:
5; Location: 5q22GeneID: 1176
50: GNB2L1 
guanine nucleotide binding protein (G protein), beta polypeptide 2-like 1 [Homo
sapiens]Other Aliases: HGNC:4399, Gnb2-rs1, H12.3, RACK1Other Designations:
protein homologous to chicken B complex protein, guanine nucleotide
bindingChromosome: 5; Location: 5q35.3GeneID: 10399
51: GABRA6 
gamma-aminobutyric acid (GABA) A receptor, alpha 6 [Homo sapiens]Other Aliases:
HGNC:4080Other Designations: gamma-aminobutyric acid A receptor, alpha
6Chromosome: 5; Location: 5q34GeneID: 2559