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| Mitochondrial disease v0.1120 | PRKN | Zornitza Stark Marked gene: PRKN as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.1120 | PRKN | Zornitza Stark Gene: prkn has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.1120 | PRKN |
Zornitza Stark changed review comment from: Parkin regulates the clearance of dysfunctional mitochondria.; to: Well established gene-disease association. Parkin regulates the clearance of dysfunctional mitochondria. |
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| Mitochondrial disease v0.1120 | PRKN | Zornitza Stark edited their review of gene: PRKN: Changed publications: 20837857 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.1120 | PRKN | Zornitza Stark edited their review of gene: PRKN: Changed phenotypes: Parkinson disease, juvenile, type 2, MIM# 600116; Changed mode of inheritance: BIALLELIC, autosomal or pseudoautosomal | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.1120 | PRKN | Zornitza Stark reviewed gene: PRKN: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: None | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.923 | PRKN |
Bryony Thompson gene: PRKN was added gene: PRKN was added to Mitochondrial disease. Sources: Expert Review Green Mode of inheritance for gene: PRKN was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: PRKN were set to 29884839; 38069350 Phenotypes for gene: PRKN were set to Disorders of mitochondrial protein quality control; Parkinson disease MONDO:0005180 |
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