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| Early-onset Parkinson disease v2.38 | KCNJ15 | Zornitza Stark Marked gene: KCNJ15 as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Early-onset Parkinson disease v2.38 | KCNJ15 | Zornitza Stark Gene: kcnj15 has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Early-onset Parkinson disease v2.38 | KCNJ15 |
Zornitza Stark gene: KCNJ15 was added gene: KCNJ15 was added to Early-onset Parkinson disease. Sources: Literature Mode of inheritance for gene: KCNJ15 was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: KCNJ15 were set to 40566643 Phenotypes for gene: KCNJ15 were set to Parkinson disease, MONDO:0005180, KCNJ15-related Review for gene: KCNJ15 was set to RED Added comment: Single multiplex family reported with a missense variant and functional data. Sources: Literature |
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