Hyperbilirubinemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0020433
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Genes

127 genes associated with the disease Hyperbilirubinemia in GWAS and other genetic association datasets from the DisGeNET Gene-Disease Associations dataset.

Symbol Name
ABCB1 ATP-binding cassette, sub-family B (MDR/TAP), member 1
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2
ABCC3 ATP-binding cassette, sub-family C (CFTR/MRP), member 3
ABCG2 ATP-binding cassette, sub-family G (WHITE), member 2 (Junior blood group)
ABO ABO blood group (transferase A, alpha 1-3-N-acetylgalactosaminyltransferase; transferase B, alpha 1-3-galactosyltransferase)
ADA adenosine deaminase
ADAMTS13 ADAM metallopeptidase with thrombospondin type 1 motif, 13
ADK adenosine kinase
AFP alpha-fetoprotein
AKR1D1 aldo-keto reductase family 1, member D1
ALAS2 5'-aminolevulinate synthase 2
ALB albumin
ALDOB aldolase B, fructose-bisphosphate
AMACR alpha-methylacyl-CoA racemase
ANK1 ankyrin 1, erythrocytic
APOE apolipoprotein E
ARNTL aryl hydrocarbon receptor nuclear translocator-like
ARR3 arrestin 3, retinal (X-arrestin)
ATP11C ATPase, class VI, type 11C
BCL2 B-cell CLL/lymphoma 2
BDNF brain-derived neurotrophic factor
BLVRA biliverdin reductase A
CALB1 calbindin 1, 28kDa
CARTPT CART prepropeptide
CASR calcium-sensing receptor
CDC50A cell division cycle 50 P4-ATPase accessory subunit A
CENPJ centromere protein J
CNDP1 carnosine dipeptidase 1 (metallopeptidase M20 family)
COG6 component of oligomeric golgi complex 6
CP ceruloplasmin (ferroxidase)
CRBN cereblon
CRP C-reactive protein, pentraxin-related
CSF3 colony stimulating factor 3 (granulocyte)
CXADR coxsackie virus and adenovirus receptor
CYP2B6 cytochrome P450, family 2, subfamily B, polypeptide 6
DGUOK deoxyguanosine kinase
ENO2 enolase 2 (gamma, neuronal)
EPB42 erythrocyte membrane protein band 4.2
EPO erythropoietin
ERLIN1 ER lipid raft associated 1
ESR1 estrogen receptor 1
F2 coagulation factor II (thrombin)
F7 coagulation factor VII (serum prothrombin conversion accelerator)
FBL fibrillarin
FH fumarate hydratase
FXN frataxin
G6PD glucose-6-phosphate dehydrogenase
GGTLC1 gamma-glutamyltransferase light chain 1
GPT glutamic-pyruvate transaminase (alanine aminotransferase)
GSTK1 glutathione S-transferase kappa 1
GSTM1 glutathione S-transferase mu 1
HAMP hepcidin antimicrobial peptide
HK1 hexokinase 1
HLA-DRB1 major histocompatibility complex, class II, DR beta 1
HMBS hydroxymethylbilane synthase
HMGB1 high mobility group box 1
HMOX1 heme oxygenase 1
HSD3B7 hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 7
IBSP integrin-binding sialoprotein
IFNG interferon, gamma
IKZF3 IKAROS family zinc finger 3 (Aiolos)
IL13 interleukin 13
IL2 interleukin 2
ITPA inosine triphosphatase (nucleoside triphosphate pyrophosphatase)
JAG1 jagged 1
KCNN4 potassium channel, calcium activated intermediate/small conductance subfamily N alpha, member 4
KIF23 kinesin family member 23
KLF1 Kruppel-like factor 1 (erythroid)
KLHL1 kelch-like family member 1
LBR lamin B receptor
LOC102724197 inactive gamma-glutamyltranspeptidase 2-like
LPL lipoprotein lipase
MT1E metallothionein 1E
MTHFR methylenetetrahydrofolate reductase (NAD(P)H)
NBN nibrin
NCOR1 nuclear receptor corepressor 1
NR1I3 nuclear receptor subfamily 1, group I, member 3
NT5C1A 5'-nucleotidase, cytosolic IA
OSTM1 osteopetrosis associated transmembrane protein 1
PAX8 paired box 8
PEX19 peroxisomal biogenesis factor 19
PGK1 phosphoglycerate kinase 1
POMC proopiomelanocortin
POR P450 (cytochrome) oxidoreductase
PPARA peroxisome proliferator-activated receptor alpha
PRKAR1A protein kinase, cAMP-dependent, regulatory, type I, alpha
PRPH2 peripherin 2 (retinal degeneration, slow)
PVALB parvalbumin
RDX radixin
RFX6 regulatory factor X, 6
RHAG Rh-associated glycoprotein
SLC10A1 solute carrier family 10 (sodium/bile acid cotransporter), member 1
SLC17A5 solute carrier family 17 (acidic sugar transporter), member 5
SLC22A7 solute carrier family 22 (organic anion transporter), member 7
SLC25A13 solute carrier family 25 (aspartate/glutamate carrier), member 13
SLC30A10 solute carrier family 30, member 10
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2
SLC4A1 solute carrier family 4 (anion exchanger), member 1 (Diego blood group)
SLCO1A2 solute carrier organic anion transporter family, member 1A2
SLCO1B1 solute carrier organic anion transporter family, member 1B1
SLCO1B3 solute carrier organic anion transporter family, member 1B3
SLCO6A1 solute carrier organic anion transporter family, member 6A1
SPG7 spastic paraplegia 7 (pure and complicated autosomal recessive)
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic
SYCE1L synaptonemal complex central element protein 1-like
TBC1D9 TBC1 domain family, member 9 (with GRAM domain)
TNF tumor necrosis factor
TRIM13 tripartite motif containing 13
TRMU tRNA 5-methylaminomethyl-2-thiouridylate methyltransferase
TST thiosulfate sulfurtransferase (rhodanese)
TTC4 tetratricopeptide repeat domain 4
UBL4A ubiquitin-like 4A
UGGT1 UDP-glucose glycoprotein glucosyltransferase 1
UGT1A1 UDP glucuronosyltransferase 1 family, polypeptide A1
UGT1A10 UDP glucuronosyltransferase 1 family, polypeptide A10
UGT1A3 UDP glucuronosyltransferase 1 family, polypeptide A3
UGT1A4 UDP glucuronosyltransferase 1 family, polypeptide A4
UGT1A5 UDP glucuronosyltransferase 1 family, polypeptide A5
UGT1A6 UDP glucuronosyltransferase 1 family, polypeptide A6
UGT1A7 UDP glucuronosyltransferase 1 family, polypeptide A7
UGT1A8 UDP glucuronosyltransferase 1 family, polypeptide A8
UGT1A9 UDP glucuronosyltransferase 1 family, polypeptide A9
UMPS uridine monophosphate synthetase
WDR35 WD repeat domain 35
XYLT2 xylosyltransferase II