prognathia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Abnormal prominence of the chin related to increased length of the mandible. (Human Phenotype Ontology, HP_0000303)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010208
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Genes

2 gene mutations causing the prognathia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FGFR3 fibroblast growth factor receptor 3
SMG1 SMG1 phosphatidylinositol 3-kinase-related kinase