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Prepair 1000+ v0.47 SHOX Zornitza Stark Marked gene: SHOX as ready
Prepair 1000+ v0.47 SHOX Zornitza Stark Gene: shox has been classified as Amber List (Moderate Evidence).
Prepair 1000+ v0.47 SHOX Zornitza Stark Mode of inheritance for gene: SHOX was changed from BIALLELIC, autosomal or pseudoautosomal to Other
Prepair 1000+ v0.46 SHOX Zornitza Stark Classified gene: SHOX as Amber List (moderate evidence)
Prepair 1000+ v0.46 SHOX Zornitza Stark Gene: shox has been classified as Amber List (Moderate Evidence).
Prepair 1000+ v0.45 SHOX Zornitza Stark Tag SV/CNV tag was added to gene: SHOX.
Prepair 1000+ v0.40 SHOX Crystle Lee reviewed gene: SHOX: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Langer mesomelic dysplasia (MIM#249700), Leri-Weill dyschondrosteosis (MIM#127300), Short stature, idiopathic familial (MIM#300582); Mode of inheritance: Other
Prepair 1000+ v0.0 SHOX Zornitza Stark gene: SHOX was added
gene: SHOX was added to Reproductive Carrier Screen_VCGS. Sources: Mackenzie's Mission,Expert Review Green
Mode of inheritance for gene: SHOX was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: SHOX were set to Langer mesomelic dysplasia, 249700 (3)