interparietal bone hypoplasia Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description underdevelopment or reduced size, usually due to a reduced number of cells, in the bone of the cranium that lies above and anterior to the occipital bone in some mammals (Mammalian Phenotype Ontology, MP_0004385)
External Link
Similar Terms
Downloads & Tools


4 gene mutations causing the interparietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
GJA1 gap junction protein, alpha 1, 43kDa
RUNX2 runt-related transcription factor 2
SC5D sterol-C5-desaturase
WDR19 WD repeat domain 19