cleft chin Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description incomplete fusion of the chin; usually a fissure (Mammalian Phenotype Ontology, MP_0000114)
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3 gene mutations causing the cleft chin phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
EDN1 endothelin 1
EDNRA endothelin receptor type A
MSX1 msh homeobox 1