Source: ALL

Gene Disease Score gda Association Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 860
Gene Symbol: RUNX2
RUNX2
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.020 GeneticVariation BEFREE These pathways also operated in vivo, as evidenced by recapitulation of RTS spectrum phenotypes with osteoblast-specific Pdk1 deletion in mice (Pdk1osx mice) and by the genetic interactions observed in mice heterozygous for both osteoblast-specific Pdk1 deletion and either Runx2 or Creb deletion. 22133875

2012
Entrez Id: 860
Gene Symbol: RUNX2
RUNX2
CUI: C0035372
Disease: Rett Syndrome
Rett Syndrome 		0.020 Biomarker BEFREE The molecular-genetic analysis of two underlying genes (CBFA1 and CBP) for CCD and RTS was performed using SSCP, direct sequencing and FISH. 12416539

2002