abnormal bile duct development Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description incomplete or aberrant differentiation of the channels that secrete bile from the liver to the gall bladder and intestines (Mammalian Phenotype Ontology, MP_0002929)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002929
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13 gene mutations causing the abnormal bile duct development phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARL3 ADP-ribosylation factor-like 3
B9D1 B9 protein domain 1
GPBAR1 G protein-coupled bile acid receptor 1
HES1 hes family bHLH transcription factor 1
JUN jun proto-oncogene
MKS1 Meckel syndrome, type 1
NOTCH2 notch 2
ONECUT1 one cut homeobox 1
ONECUT2 one cut homeobox 2
PDX1 pancreatic and duodenal homeobox 1
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
SOX17 SRY (sex determining region Y)-box 17