Hyperbilirubinemia, Neonatal Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
External Link https://www.disgenet.org/browser/0/1/0/C0857007
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Genes

32 genes associated with the disease Hyperbilirubinemia, Neonatal 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
ALB albumin
BLVRA biliverdin reductase A
CAT catalase
EPB41 erythrocyte membrane protein band 4.1
FBP1 fructose-1,6-bisphosphatase 1
G6PD glucose-6-phosphate dehydrogenase
GPX1 glutathione peroxidase 1
GSTK1 glutathione S-transferase kappa 1
GYPC glycophorin C (Gerbich blood group)
HMOX1 heme oxygenase 1
HPGDS hematopoietic prostaglandin D synthase
IGF1 insulin-like growth factor 1 (somatomedin C)
IKBKB inhibitor of kappa light polypeptide gene enhancer in B-cells, kinase beta
NCOR1 nuclear receptor corepressor 1
NR1I3 nuclear receptor subfamily 1, group I, member 3
SLC35A2 solute carrier family 35 (UDP-galactose transporter), member A2
SLCO1B1 solute carrier organic anion transporter family, member 1B1
SLCO6A1 solute carrier organic anion transporter family, member 6A1
SPTA1 spectrin, alpha, erythrocytic 1
SPTB spectrin, beta, erythrocytic
UBE2A ubiquitin-conjugating enzyme E2A
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