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| Mitochondrial disease v0.993 | FAM136A | Zornitza Stark Marked gene: FAM136A as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.993 | FAM136A | Zornitza Stark Gene: fam136a has been classified as Red List (Low Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.993 | FAM136A |
Zornitza Stark gene: FAM136A was added gene: FAM136A was added to Mitochondrial disease. Sources: Literature Mode of inheritance for gene: FAM136A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted Publications for gene: FAM136A were set to 40714634 Phenotypes for gene: FAM136A were set to Meniere's disease Review for gene: FAM136A was set to RED Added comment: Single family reported with high impact variant, supportive functional data. Sources: Literature |
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