parietal 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 curved bone forming part of the vault of the cranium (Mammalian Phenotype Ontology, MP_0004420)
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4 gene mutations causing the parietal bone hypoplasia phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BNC2 basonuclin 2
ITGB1BP1 integrin beta 1 binding protein 1
RUNX2 runt-related transcription factor 2
WDR19 WD repeat domain 19