1: SLC14A1 
solute carrier family 14 (urea transporter), member 1 (Kidd blood group) [Homo
sapiens]Other Aliases: HGNC:10918, HsT1341, JK, RACH1, UT-B1, UT1, UTEOther
Designations: RACH1; Solute carrier family 14 (urea transporter), member 1 (Kidd
bloodChromosome: 18; Location: 18q11-q12GeneID: 6563
2: SLC39A6 
solute carrier family 39 (zinc transporter), member 6 [Homo sapiens]Other
Aliases: HGNC:18607, LIV-1Other Designations: LIV-1 protein, estrogen regulated;
solute carrier family 39 (metal ion transporter), member 6Chromosome: 18;
Location: 18q12.2GeneID: 25800
3: SLC14A2 
solute carrier family 14 (urea transporter), member 2 [Homo sapiens]Other
Aliases: HGNC:10919, HUT2, UT2, UTROther Designations: Urea
transporter-2Chromosome: 18; Location: 18q12.1-q21.1GeneID: 8170
4: NPC1 
Niemann-Pick disease, type C1 [Homo sapiens]Other Aliases: HGNC:7897,
NPCChromosome: 18; Location: 18q11-q12GeneID: 4864
5: TXNL4A 
thioredoxin-like 4A [Homo sapiens]Other Aliases: HGNC:30551, DIM1, HsT161,
TXNL4, U5-15kDOther Designations: thioredoxin-like 4Chromosome: 18; Location:
18q23GeneID: 10907
6: NAPG 
N-ethylmaleimide-sensitive factor attachment protein, gamma [Homo sapiens]Other
Aliases: HGNC:7642, GAMMASNAPOther Designations: gamma SNAP; soluble NSF
attachment proteinChromosome: 18; Location: 18p11.22GeneID: 8774
7: SYT4 
synaptotagmin IV [Homo sapiens]Other Aliases: HGNC:11512, HsT1192, KIAA1342Other
Designations: synaptotagmin 4Chromosome: 18; Location: 18q12.3GeneID: 6860
8: C18orf26 
chromosome 18 open reading frame 26 [Homo sapiens]Other Aliases: HGNC:26808,
FLJ39106Chromosome: 18; Location: 18q21.2GeneID: 284254
9: TXNL1 
thioredoxin-like 1 [Homo sapiens]Other Aliases: HGNC:12436, TRP32, TXNL,
TxlOther Designations: thioredoxin-like, 32kD; thioredoxin-like, 32kDa;
thioredoxin-related 32 kDa proteinChromosome: 18; Location: 18q21.2GeneID: 9352
10: TTR 
transthyretin (prealbumin, amyloidosis type I) [Homo sapiens]Other Aliases:
HGNC:12405, HsT2651, PALB, TBPAOther Designations: prealbumin;
transthyretinChromosome: 18; Location: 18q12.1GeneID: 7276
11: AQP4 
aquaporin 4 [Homo sapiens]Other Aliases: HGNC:637, HMIWC2, MGC22454, MIWCOther
Designations: mercurial-insensitive water channelChromosome: 18; Location:
18q11.2-q12.1GeneID: 361
12: FLJ20793 
FLJ20793 protein [Homo sapiens]Other Aliases: KIAA1830Chromosome: 18; Location:
18q22GeneID: 54495
13: KIAA1012 
KIAA1012 [Homo sapiens]Other Aliases: HGNC:29169, HsT2706Chromosome: 18;
Location: 18q12.1GeneID: 22878
14: ME2 
malic enzyme 2, NAD(+)-dependent, mitochondrial [Homo sapiens]Other Aliases:
HGNC:6984Other Designations: Malic enzyme, mitochondrial; malate dehydrogenase;
malic enzyme 2, mitochondrial; pyruvic-malic carboxylaseChromosome: 18;
Location: 18q21GeneID: 4200
15: ATP5A1 
ATP synthase, H+ transporting, mitochondrial F1 complex, alpha subunit, isoform
1, cardiac muscle [Homo sapiens]Other Aliases: HGNC:823, ATP5A, ATP5AL2, ATPM,
OMR, ORM, hATP1Other Designations: ATP synthase alpha chain, mitochondrial; ATP
synthase, H+ transporting, mitochondrial F1 complex, alpha subunit; ATP
synthase, H+ transporting, mitochondrial F1 complex, alpha subunit, isoform 2,
non-cardiac muscle-like 2; mitochondrial ATP synthetase,
oligomycin-resistantChromosome: 18; Location: 18q12-q21GeneID: 498
16: ZFP161 
zinc finger protein 161 homolog (mouse) [Homo sapiens]Other Aliases: HGNC:12860,
ZBTB14, ZF5, ZNF478Other Designations: zinc finger protein 161 homolog; zinc
finger protein homologous to Zfp161 in mouseChromosome: 18; Location:
18pter-p11.2GeneID: 7541
17: ATP8B1 
ATPase, Class I, type 8B, member 1 [Homo sapiens]Other Aliases: HGNC:3706,
ATPIC, BRIC, FIC1, PFIC, PFIC1Other Designations: ATPase ,Class I, type 8B,
member 1; benign recurrent intrahepatic cholestasis; familial intrahepatic
cholestasis 1, (progressive, Byler disease and benign recurrent); progressive
familial intrahepatic cholestasis 1, Byler diseaseChromosome: 18; Location:
18q21GeneID: 5205