1: SLC16A2 
solute carrier family 16 (monocarboxylic acid transporters), member 2 [Homo
sapiens]Other Aliases: HGNC:10923, DXS128, DXS128E, MCT8, XPCTOther
Designations: X-linked PEST-containing transporter; monocarboxylate transporter
8; solute carrier family 16 (monocarboxylic acid transporters), member 2
(putative transporter); solute carrier family 16, member 2Chromosome: X;
Location: Xq13.2GeneID: 6567
2: SLC35A2 
solute carrier family 35 (UDP-galactose transporter), member A2 [Homo
sapiens]Other Aliases: HGNC:11022, UGALT, UGAT, UGT, UGT1, UGT2, UGTLOther
Designations: UDP-galactose translocator; solute carrier family 35
(UDP-galactose transporter), member 2Chromosome: X; Location:
Xp11.23-p11.22GeneID: 7355
3: SLC6A14 
solute carrier family 6 (neurotransmitter transporter), member 14 [Homo
sapiens]Other Aliases: HGNC:11047, ATB(0+), OBXOther Designations: amino acid
transporter B0+Chromosome: X; Location: Xq23-q24GeneID: 11254
4: LOC441515 
similar to Sodium- and chloride-dependent neutral and basic amino acid
transporter B(0+) (Amino acid transporter ATB0+) (Solute carrier family 6 member
14) [Homo sapiens]Chromosome: X; Location: Xq23GeneID: 441515
5: SLC6A8 
solute carrier family 6 (neurotransmitter transporter, creatine), member 8 [Homo
sapiens]Other Aliases: HGNC:11055, CRTR, CT1Chromosome: X; Location: Xq28GeneID:
6535
6: SLC7A3 
solute carrier family 7 (cationic amino acid transporter, y+ system), member 3
[Homo sapiens]Other Aliases: HGNC:11061, ATRC3, CAT-3, FLJ14541Chromosome: X;
Location: Xq13.1GeneID: 84889
7: LOC286408 
similar to putative UST1-like organic anion transporter [Homo
sapiens]Chromosome: X; Location: Xp11.23GeneID: 286408
8: ATP7A 
ATPase, Cu++ transporting, alpha polypeptide (Menkes syndrome) [Homo
sapiens]Other Aliases: HGNC:869, MK, MNK, OHSOther Designations: ATPase, Cu++
transporting, alpha polypeptide; Menkes disease-associated protein; copper pump
1; copper-transporting ATPase 1Chromosome: X; Location: Xq13.2-q13.3GeneID: 538
9: XK 
Kell blood group precursor (McLeod phenotype) [Homo sapiens]Other Aliases:
HGNC:12811, KXOther Designations: McLeod syndrome-associated, Kell blood group
protein; membrane transport proteinChromosome: X; Location: Xp21.1GeneID: 7504
10: SLC25A5 
solute carrier family 25 (mitochondrial carrier; adenine nucleotide
translocator), member 5 [Homo sapiens]Other Aliases: HGNC:10991, 2F1, ANT2, T2,
T3Other Designations: adenine nucleotide translocator 2 (fibroblast); solute
carrier family 25, member 5Chromosome: X; Location: Xq24-q26GeneID: 292
11: ABCD1 
ATP-binding cassette, sub-family D (ALD), member 1 [Homo sapiens]Other Aliases:
HGNC:61, ABC42, ALD, ALDP, AMNOther Designations: adrenoleukodystrophy;
adrenoleukodystrophy proteinChromosome: X; Location: Xq28GeneID: 215
12: SYTL4 
synaptotagmin-like 4 (granuphilin-a) [Homo sapiens]Other Aliases:
HGNC:15588Other Designations: granuphilin-aChromosome: XGeneID: 94121
13: NXF3 
nuclear RNA export factor 3 [Homo sapiens]Other Aliases: HGNC:8073Chromosome: X;
Location: Xq22-q23GeneID: 56000
14: NXT2 
nuclear transport factor 2-like export factor 2 [Homo sapiens]Other Aliases:
HGNC:18151, P15-2Chromosome: X; Location: Xq23GeneID: 55916
15: EBP 
emopamil binding protein (sterol isomerase) [Homo sapiens]Other Aliases:
HGNC:3133, CDPX2, CHO2, CPX, CPXDOther Designations:
3-beta-hydroxysteroid-delta-8,delta-7-isomerase; Chondrodysplasia punctata-2,
X-linked dominant (Happle syndrome); emopamil-binding protein (sterol
isomerase); sterol 8-isomeraseChromosome: X; Location: Xp11.23-p11.22GeneID:
10682
16: GLUD2 
glutamate dehydrogenase 2 [Homo sapiens]Other Aliases: HGNC:4336, GLUDP1Other
Designations: glutamate dehydrogenase pseudogene 1Chromosome: X; Location:
Xq24-q25GeneID: 2747
17: SLC25A6 
solute carrier family 25 (mitochondrial carrier; adenine nucleotide
translocator), member 6 [Homo sapiens]Other Aliases: HGNC:10992, ANT3, ANT3Y,
MGC17525Other Designations: ADP,ATP carrier protein, liver isoform T2; ADP/ATP
translocase 3; ADP/ATP translocator of liver; adenine nucleotide translocator 3;
solute carrier family 25, member A6Chromosome: X, Y; Location: Xp22.32 and
YpGeneID: 293
18: DKFZp564K142 
implantation-associated protein [Homo sapiens]Other Aliases: FLJ14726,
PRO0756Chromosome: X; Location: Xq21.1GeneID: 84061
19: GABRQ 
gamma-aminobutyric acid (GABA) receptor, theta [Homo sapiens]Other Aliases:
HGNC:14454, THETAOther Designations: GABA-A receptor theta subunitChromosome: X;
Location: Xq28GeneID: 55879
20: AP1S2 
adaptor-related protein complex 1, sigma 2 subunit [Homo sapiens]Other Aliases:
HGNC:560, DC22, MGC:1902, SIGMA1BOther Designations: Golgi adaptor HA1/AP1
adaptin sigma 1B subunit; adaptor-related protein complex 1 sigma 2 subunit;
clathrin adaptor complex AP1 sigma 1B subunit; clathrin assembly protein complex
1 sigma-1B small chain; clathrin-associated/assembly/adaptor protein small
1-likeChromosome: X; Location: Xp22.2GeneID: 8905
21: SYN1 
synapsin I [Homo sapiens]Other Aliases: HGNC:11494, SYN1a, SYN1b, SYNIOther
Designations: brain protein 4.1Chromosome: X; Location: Xp11.23GeneID: 6853
22: MAOB 
monoamine oxidase B [Homo sapiens]Other Aliases: HGNC:6834, MGC26382Other
Designations: MAO, brain; MAO, platelet; adrenalin oxidase; amine oxidase
(flavin-containing); tyramine oxidaseChromosome: X; Location: Xp11.23GeneID:
4129
23: ABCB7 
ATP-binding cassette, sub-family B (MDR/TAP), member 7 [Homo sapiens]Other
Aliases: HGNC:48, ABC7, ASAT, Atm1p, EST140535Other Designations: ATP-binding
cassette 7; ATP-binding cassette, sub-family B, member 7; Anemia, sideroblastic,
with spinocerebellar ataxiaChromosome: X; Location: Xq12-q13GeneID: 22
24: LOC203427 
similar to solute carrier family 25 , member 16 [Homo sapiens]Other
Designations: mitochondrial solute carrier proteinChromosome: X; Location:
Xq24GeneID: 203427
25: SLC38A5 
solute carrier family 38, member 5 [Homo sapiens]Other Aliases: HGNC:18070,
JM24, SN2Other Designations: amino acid transport system N2Chromosome: X;
Location: Xp11.23GeneID: 92745
26: RNF127 
ring finger protein 127 [Homo sapiens]Other Aliases: HGNC:21152,
FLJ22612Chromosome: X; Location: Xq24GeneID: 79836
27: UPF3B 
UPF3 regulator of nonsense transcripts homolog B (yeast) [Homo sapiens]Other
Aliases: HGNC:20439, HUPF3B, RENT3B, UPF3XOther Designations: UPF3 regulator of
nonsense transcripts homolog BChromosome: X; Location: Xq25-q26GeneID: 65109
28: NXF2 
nuclear RNA export factor 2 [Homo sapiens]Other Aliases: HGNC:8072, FLJ20416,
TAPL-2Other Designations: TAP like protein 2Chromosome: X; Location:
Xq22.1GeneID: 56001
29: FLJ20298 
FLJ20298 protein [Homo sapiens]Chromosome: X; Location: Xq22.3GeneID: 54885
30: ATP1B4 
ATPase, (Na+)/K+ transporting, beta 4 polypeptide [Homo sapiens]Other Aliases:
HGNC:808Other Designations: X,K-ATPase beta-m subunitChromosome: X; Location:
Xq24GeneID: 23439
31: SYP 
synaptophysin [Homo sapiens]Other Aliases: HGNC:11506Other Designations: major
synaptic vesicle protein P38Chromosome: X; Location: Xp11.23-p11.22GeneID: 6855
32: SEDL 
spondyloepiphyseal dysplasia, late [Homo sapiens]Other Aliases: HGNC:10709,
SEDTOther Designations: sedlinChromosome: X; Location: Xp22GeneID: 6399
33: PLP2 
proteolipid protein 2 (colonic epithelium-enriched) [Homo sapiens]Other Aliases:
HGNC:9087, A4, A4-LSBOther Designations: A4 differentiation-dependent
proteinChromosome: X; Location: Xp11.23GeneID: 5355
34: GRIA3 
glutamate receptor, ionotrophic, AMPA 3 [Homo sapiens]Other Aliases: HGNC:4573,
GLUR-K3, GLUR3, GLURCOther Designations: glutamate receptor 3Chromosome: X;
Location: Xq25-q26GeneID: 2892
35: CYBB 
cytochrome b-245, beta polypeptide (chronic granulomatous disease) [Homo
sapiens]Other Aliases: HGNC:2578, CGD, GP91-1, GP91-PHOX, GP91PHOX,
NOX2Chromosome: X; Location: Xp21.1GeneID: 1536
36: ATP6AP1 
ATPase, H+ transporting, lysosomal accessory protein 1 [Homo sapiens]Other
Aliases: HGNC:868, 16A, ATP6IP1, ATP6S1, Ac45, CF2, ORF, VATPS1, XAP-3,
XAP3Other Designations: ATPase, H+ transporting, lysosomal (vacuolar proton
pump), subunit 1; ATPase, H+ transporting, lysosomal interacting protein 1;
H-ATPase subunit; V-ATPase S1 accessory proteinChromosome: X; Location:
Xq28GeneID: 537