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Osteopetrosis v1.0 CLCN7 Sangavi Sivagnanasundram changed review comment from: Both AD and AR GDA has been classified as DEFINITIVE by ClinGen Skeletal Dysplasia GCEP in 2023

AD - https://search.clinicalgenome.org/CCID:004466
AR - https://search.clinicalgenome.org/CCID:004467; to: Both AD and AR GDA has been classified as DEFINITIVE by ClinGen Skeletal Dysplasia GCEP in 2023

AD - https://search.clinicalgenome.org/CCID:004466 - Dominant negative MOD
AR - https://search.clinicalgenome.org/CCID:004467 - Loss of function MOD
Osteopetrosis v1.0 CLCN7 Sangavi Sivagnanasundram reviewed gene: CLCN7: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: autosomal dominant osteopetrosis 2 MONDO:0008156, autosomal recessive osteopetrosis 4 MONDO:0012676; Mode of inheritance: BOTH monoallelic and biallelic (but BIALLELIC mutations cause a more SEVERE disease form), autosomal or pseudoautosomal
Osteopetrosis v0.29 CLCN7 Zornitza Stark Marked gene: CLCN7 as ready
Osteopetrosis v0.29 CLCN7 Zornitza Stark Gene: clcn7 has been classified as Green List (High Evidence).
Osteopetrosis v0.29 CLCN7 Zornitza Stark Phenotypes for gene: CLCN7 were changed from to Osteopetrosis, autosomal recessive 4, MIM#611490
Osteopetrosis v0.28 CLCN7 Zornitza Stark Publications for gene: CLCN7 were set to
Osteopetrosis v0.27 CLCN7 Zornitza Stark Mode of inheritance for gene: CLCN7 was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Osteopetrosis v0.26 CLCN7 Zornitza Stark Tag treatable tag was added to gene: CLCN7.
Osteopetrosis v0.0 CLCN7 Zornitza Stark gene: CLCN7 was added
gene: CLCN7 was added to Osteopetrosis_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: CLCN7 was set to Unknown