Unconjugated Hyperbilirubinemia Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description An increased amount of unconjugated (indirect) bilurubin in the blood. (Human Phenotype Ontology, HP_0008282)
External Link https://www.disgenet.org/browser/0/1/0/C0268306
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Genes

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

Symbol Name
CASK calcium/calmodulin-dependent serine protein kinase (MAGUK family)
G6PD glucose-6-phosphate dehydrogenase
GSTM1 glutathione S-transferase mu 1
HBB hemoglobin, beta
HMOX1 heme oxygenase 1
IDH1 isocitrate dehydrogenase 1 (NADP+), soluble
IDH2 isocitrate dehydrogenase 2 (NADP+), mitochondrial
PKLR pyruvate kinase, liver and RBC
RHAG Rh-associated glycoprotein
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2
SLCO1B1 solute carrier organic anion transporter family, member 1B1
SLCO1B3 solute carrier organic anion transporter family, member 1B3
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