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Dystonia - isolated/combined v0.22 | KCTD17 | Zornitza Stark Marked gene: KCTD17 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Dystonia - isolated/combined v0.22 | KCTD17 | Zornitza Stark Gene: kctd17 has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Dystonia - isolated/combined v0.22 | KCTD17 | Zornitza Stark Phenotypes for gene: KCTD17 were changed from Dystonia 26, myoclonic to Dystonia 26, myoclonic MIM#616398 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Dystonia - isolated/combined v0.21 | KCTD17 | Zornitza Stark Publications for gene: KCTD17 were set to | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Dystonia - isolated/combined v0.6 | KCTD17 | Bryony Thompson edited their review of gene: KCTD17: Changed rating: GREEN | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Dystonia - isolated/combined v0.6 | KCTD17 | Bryony Thompson reviewed gene: KCTD17: Rating: ; Mode of pathogenicity: None; Publications: 25983243, 30642807, 30579817; Phenotypes: Dystonia 26, myoclonic MIM#616398; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Dystonia - isolated/combined v0.0 | KCTD17 |
Bryony Thompson gene: KCTD17 was added gene: KCTD17 was added to Dystonia - isolated/combined_RMH. Sources: Royal Melbourne Hospital,Expert Review Green Mode of inheritance for gene: KCTD17 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Phenotypes for gene: KCTD17 were set to Dystonia 26, myoclonic |