abnormality of the parietal bone Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description Any abnormality of the parietal bone of the skull. (Human Phenotype Ontology, HP_0002696)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0002696
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Genes

11 genes associated with the abnormality of the parietal bone phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALX4 ALX homeobox 4
CREBBP CREB binding protein
FGFR2 fibroblast growth factor receptor 2
MSX2 msh homeobox 2
PTCH1 patched 1
PTCH2 patched 2
PTPN11 protein tyrosine phosphatase, non-receptor type 11
RPS19 ribosomal protein S19
RUNX2 runt-related transcription factor 2
SUFU suppressor of fused homolog (Drosophila)
TWIST1 twist family bHLH transcription factor 1
Funding