abnormal bile duct physiology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any functional anomaly of the channels that secrete bile from the liver to the gall bladder and intestines (Mammalian Phenotype Ontology, MP_0003252)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003252
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22 gene mutations causing the abnormal bile duct physiology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ABCB11 ATP-binding cassette, sub-family B (MDR/TAP), member 11
ABCB4 ATP-binding cassette, sub-family B (MDR/TAP), member 4
ABCC2 ATP-binding cassette, sub-family C (CFTR/MRP), member 2
ABCG5 ATP-binding cassette, sub-family G (WHITE), member 5
ADA adenosine deaminase
AHR aryl hydrocarbon receptor
ARL3 ADP-ribosylation factor-like 3
ATP8B1 ATPase, aminophospholipid transporter, class I, type 8B, member 1
ATXN2 ataxin 2
CYP8B1 cytochrome P450, family 8, subfamily B, polypeptide 1
MAP3K14 mitogen-activated protein kinase kinase kinase 14
NR1H4 nuclear receptor subfamily 1, group H, member 4
P2RY13 purinergic receptor P2Y, G-protein coupled, 13
PCTP phosphatidylcholine transfer protein
PEX1 peroxisomal biogenesis factor 1
PEX2 peroxisomal biogenesis factor 2
PKD1 polycystic kidney disease 1 (autosomal dominant)
PKD2 polycystic kidney disease 2 (autosomal dominant)
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
SCP2 sterol carrier protein 2
SIK3 SIK family kinase 3
STARD10 StAR-related lipid transfer (START) domain containing 10