Hepatobiliary Disease Gene Set

Dataset DisGeNET Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A gastrointestinal system disease that is located_in the liver and/or biliary tract. (Human Disease Ontology, DOID_3118)
External Link https://www.disgenet.org/browser/0/1/0/C0267792
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Genes

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

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
AKR1B1 aldo-keto reductase family 1, member B1 (aldose reductase)
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
FBN2 fibrillin 2
FDXR ferredoxin reductase
FECH ferrochelatase
KMT2B lysine (K)-specific methyltransferase 2B
KMT2D lysine (K)-specific methyltransferase 2D
NR1H4 nuclear receptor subfamily 1, group H, member 4
SERPINA1 serpin peptidase inhibitor, clade A (alpha-1 antiproteinase, antitrypsin), member 1
TJP2 tight junction protein 2
TP53 tumor protein p53