Gene: RUNX2 ×
Source: ALL
Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 860
Gene Symbol: RUNX2
RUNX2 		0.010 GeneticVariation group BEFREE Cleidocranial dysplasia with severe parietal bone dysplasia: C-terminal RUNX2 mutations. 16463420 2006