absent gallbladder Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description A developmental defect in which the gallbladder fails to form. (Human Phenotype Ontology, HP_0011467)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003250
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Genes

3 gene mutations causing the absent gallbladder phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
HES1 hes family bHLH transcription factor 1
HLX H2.0-like homeobox
ONECUT1 one cut homeobox 1