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| Mitochondrial disease v0.1126 | TMEM126A | Zornitza Stark Marked gene: TMEM126A as ready | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.1126 | TMEM126A | Zornitza Stark Gene: tmem126a has been classified as Green List (High Evidence). | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.1126 | TMEM126A | Zornitza Stark Publications for gene: TMEM126A were set to 29884839; 33879611 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.1125 | TMEM126A |
Zornitza Stark changed review comment from: Association with OA: More than 5 unrelated families reported, functional data. Only a single family reported with deafness in addition to OA.; to: Association with OA: More than 5 unrelated families reported, functional data. Only a single family reported with deafness in addition to OA. TMEM126A is a Complex I assembly factor. |
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| Mitochondrial disease v0.1125 | Zornitza Stark Added reviews for gene TMEM126A from panel Mendeliome | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| Mitochondrial disease v0.923 | TMEM126A |
Bryony Thompson gene: TMEM126A was added gene: TMEM126A was added to Mitochondrial disease. Sources: Expert Review Green Mode of inheritance for gene: TMEM126A was set to BIALLELIC, autosomal or pseudoautosomal Publications for gene: TMEM126A were set to 29884839; 33879611 Phenotypes for gene: TMEM126A were set to Disorders of complex I subunits and assembly factors; autosomal recessive optic atrophy, OPA7 type MONDO:0013069 |
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