abnormal gallbladder morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A structural anomaly of the gallbladder. (Human Phenotype Ontology, HP_0012437)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0005084
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19 gene mutations causing the abnormal gallbladder morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ARL3 ADP-ribosylation factor-like 3
BICC1 BicC family RNA binding protein 1
CCKAR cholecystokinin A receptor
CFTR cystic fibrosis transmembrane conductance regulator (ATP-binding cassette sub-family C, member 7)
CHUK conserved helix-loop-helix ubiquitous kinase
FREM1 FRAS1 related extracellular matrix 1
GPBAR1 G protein-coupled bile acid receptor 1
GUCY1B3 guanylate cyclase 1, soluble, beta 3
HES1 hes family bHLH transcription factor 1
HLX H2.0-like homeobox
KLB klotho beta
NPC1L1 NPC1-like 1
NR1H4 nuclear receptor subfamily 1, group H, member 4
ONECUT1 one cut homeobox 1
PKHD1 polycystic kidney and hepatic disease 1 (autosomal recessive)
SIK3 SIK family kinase 3
SOX7 SRY (sex determining region Y)-box 7
THBS1 thrombospondin 1
VTI1B vesicle transport through interaction with t-SNAREs 1B