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Radial Ray Abnormalities v2.0 SHOX downstream regulatory region Region SHOX downstream regulatory region migrated (gene set migration)
Radial Ray Abnormalities v2.0 SHOX Gene migrated from ENSG00000185960 to ENSG00000185960 (gene set migration)
Radial Ray Abnormalities v1.23 SHOX downstream regulatory region Sarah Milton Classified Region: SHOX downstream regulatory region as Green List (high evidence)
Radial Ray Abnormalities v1.23 SHOX downstream regulatory region Sarah Milton Region: shox downstream regulatory region has been classified as Green List (High Evidence).
Radial Ray Abnormalities v1.22 Sarah Milton Copied Region SHOX downstream regulatory region from panel Mendeliome
Radial Ray Abnormalities v1.22 SHOX downstream regulatory region Sarah Milton Region: SHOX downstream regulatory region was added
Region: SHOX downstream regulatory region was added to Radial Ray Abnormalities. Sources: Literature
regulatory region tags were added to Region: SHOX downstream regulatory region.
Mode of inheritance for Region: SHOX downstream regulatory region was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Publications for Region: SHOX downstream regulatory region were set to PMID: 30250174; 22791839; 23636926; 20301394
Phenotypes for Region: SHOX downstream regulatory region were set to Leri-Weill dyschondrosteosis (MIM#127300); Short stature, idiopathic familial (MIM#300582)
Penetrance for Region: SHOX downstream regulatory region were set to Incomplete
Radial Ray Abnormalities v0.28 SHOX Zornitza Stark Marked gene: SHOX as ready
Radial Ray Abnormalities v0.28 SHOX Zornitza Stark Gene: shox has been classified as Green List (High Evidence).
Radial Ray Abnormalities v0.28 SHOX Zornitza Stark Classified gene: SHOX as Green List (high evidence)
Radial Ray Abnormalities v0.28 SHOX Zornitza Stark Gene: shox has been classified as Green List (High Evidence).
Radial Ray Abnormalities v0.27 SHOX Zornitza Stark gene: SHOX was added
gene: SHOX was added to Radial Ray Abnormalities. Sources: Expert list
Mode of inheritance for gene: SHOX was set to X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)
Phenotypes for gene: SHOX were set to Leri-Weill dyschondrosteosis, MIM# 127300; Langer mesomelic dysplasia, MIM#249700
Review for gene: SHOX was set to GREEN
Added comment: Well established gene-disease association, radial ray abnormalities are a key feature.
Sources: Expert list