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Ataxia - adult onset v0.163 | PRKCG | Zornitza Stark Marked gene: PRKCG as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ataxia - adult onset v0.163 | PRKCG | Zornitza Stark Gene: prkcg has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ataxia - adult onset v0.163 | PRKCG | Zornitza Stark Phenotypes for gene: PRKCG were changed from Spinocerebellar ataxia 14; Spincocerebellar ataxia 14, 605361 to Spinocerebellar ataxia 14 MIM#605361 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ataxia - adult onset v0.162 | PRKCG | Zornitza Stark Publications for gene: PRKCG were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ataxia - adult onset v0.161 | PRKCG | Zornitza Stark Mode of pathogenicity for gene: PRKCG was changed from to Other | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ataxia - adult onset v0.160 | PRKCG | Zornitza Stark Mode of inheritance for gene: PRKCG was changed from MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ataxia - adult onset v0.159 | PRKCG | Michelle Torres reviewed gene: PRKCG: Rating: GREEN; Mode of pathogenicity: Other; Publications: 25217572, 18577575, 31158466; Phenotypes: Spinocerebellar ataxia 14 MIM#605361; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Ataxia - adult onset v0.0 | PRKCG |
Bryony Thompson gene: PRKCG was added gene: PRKCG was added to Ataxia - adult onset_RMH. Sources: Expert Review Green,Royal Melbourne Hospital Mode of inheritance for gene: PRKCG was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: PRKCG were set to Spinocerebellar ataxia 14; Spincocerebellar ataxia 14, 605361 |