abnormal bile duct morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly of the channels that secrete bile from the liver to the gall bladder and intestines (Mammalian Phenotype Ontology, MP_0002928)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002928
Similar Terms
Downloads & Tools


28 gene mutations causing the abnormal bile duct morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ARL3 ADP-ribosylation factor-like 3
B9D1 B9 protein domain 1
BICC1 BicC family RNA binding protein 1
CHD2 chromodomain helicase DNA binding protein 2
CYS1 cystin 1
FOXM1 forkhead box M1
GPBAR1 G protein-coupled bile acid receptor 1
HES1 hes family bHLH transcription factor 1
IFT88 intraflagellar transport 88
JUN jun proto-oncogene
MAP3K14 mitogen-activated protein kinase kinase kinase 14
MKS1 Meckel syndrome, type 1
NCF1 neutrophil cytosolic factor 1
NDFIP1 Nedd4 family interacting protein 1
NOTCH2 notch 2
ONECUT1 one cut homeobox 1
ONECUT2 one cut homeobox 2
PDX1 pancreatic and duodenal homeobox 1
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
RELB v-rel avian reticuloendotheliosis viral oncogene homolog B
RTN4RL1 reticulon 4 receptor-like 1
SOX17 SRY (sex determining region Y)-box 17
THBS1 thrombospondin 1
TNIP1 TNFAIP3 interacting protein 1