abnormal bile secretion Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the quantity or rate of bile secreted through the bile ducts in a given length of time (Mammalian Phenotype Ontology, MP_0004772)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004772
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Genes

11 gene mutations causing the abnormal bile secretion 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
ATP8B1 ATPase, aminophospholipid transporter, class I, type 8B, member 1
CYP8B1 cytochrome P450, family 8, subfamily B, polypeptide 1
NR1H4 nuclear receptor subfamily 1, group H, member 4
P2RY13 purinergic receptor P2Y, G-protein coupled, 13
PCTP phosphatidylcholine transfer protein
SCP2 sterol carrier protein 2
STARD10 StAR-related lipid transfer (START) domain containing 10