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Fetal anomalies v0.3763 RUNX2 Zornitza Stark Marked gene: RUNX2 as ready
Fetal anomalies v0.3763 RUNX2 Zornitza Stark Gene: runx2 has been classified as Green List (High Evidence).
Fetal anomalies v0.3763 RUNX2 Zornitza Stark Phenotypes for gene: RUNX2 were changed from CLEIDOCRANIAL DYSPLASIA to Cleidocranial dysplasia MIM#119600; Cleidocranial dysplasia, forme fruste, with brachydactyly MIM#119600
Fetal anomalies v0.3762 RUNX2 Zornitza Stark Publications for gene: RUNX2 were set to
Fetal anomalies v0.3761 RUNX2 Zornitza Stark Mode of inheritance for gene: RUNX2 was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Fetal anomalies v0.3721 RUNX2 Ain Roesley reviewed gene: RUNX2: Rating: GREEN; Mode of pathogenicity: None; Publications: 20301686; Phenotypes: Cleidocranial dysplasia MIM#119600, Cleidocranial dysplasia, forme fruste, with brachydactyly MIM#119600; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Fetal anomalies v0.0 RUNX2 Zornitza Stark gene: RUNX2 was added
gene: RUNX2 was added to Fetal anomalies. Sources: Expert Review Green,Genomics England PanelApp
Mode of inheritance for gene: RUNX2 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: RUNX2 were set to CLEIDOCRANIAL DYSPLASIA