primary biliary cirrhosis Gene Set

Dataset GAD Gene-Disease Associations
Category disease or phenotype associations
Type disease
Description A liver cirrhosis characterized by chronic and slow progressive destruction of intrahepatic bile ducts. (Human Disease Ontology, DOID_12236)
Similar Terms
Downloads & Tools


10 genes associated with the disease primary biliary cirrhosis in GWAS and other genetic association datasets from the GAD Gene-Disease Associations dataset.

Symbol Name
ARL14 ADP-ribosylation factor-like 14
BTNL2 butyrophilin-like 2
C6ORF10 chromosome 6 open reading frame 10
HLA-DPB1 major histocompatibility complex, class II, DP beta 1
HLA-DQB1 major histocompatibility complex, class II, DQ beta 1
IKZF3 IKAROS family zinc finger 3 (Aiolos)
IL12A interleukin 12A
IL12RB2 interleukin 12 receptor, beta 2
MBL2 mannose-binding lectin (protein C) 2, soluble
VDR vitamin D (1,25- dihydroxyvitamin D3) receptor