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Mitochondrial disorders v4.131 TRIT1 Eleanor Williams Phenotypes for gene: TRIT1 were changed from Combined oxidative phosphorylation deficiency 35, OMIM:617873 to Combined oxidative phosphorylation deficiency 35, OMIM:617873; combined oxidative phosphorylation deficiency 35, MONDO:0054742
Mitochondrial disorders v2.103 TRIT1 Eleanor Williams Phenotypes for gene: TRIT1 were changed from Combined oxidative phosphorylation deficiency 35 617873 to Combined oxidative phosphorylation deficiency 35, OMIM:617873
Mitochondrial disorders v2.102 TRIT1 Eleanor Williams Tag gene-checked tag was added to gene: TRIT1.
Mitochondrial disorders v1.216 TRIT1 Sarah Leigh Classified gene: TRIT1 as Green List (high evidence)
Mitochondrial disorders v1.216 TRIT1 Sarah Leigh Added comment: Comment on list classification: Associated with relevant phenotype in OMIM and as possible Gen2Phen gene. At least 6 variants reported in at least 6 unrelated cases.
Mitochondrial disorders v1.216 TRIT1 Sarah Leigh Gene: trit1 has been classified as Green List (High Evidence).
Mitochondrial disorders v1.215 TRIT1 Sarah Leigh Mode of inheritance for gene: TRIT1 was changed from to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v1.214 TRIT1 Sarah Leigh Publications for gene: TRIT1 were set to
Mitochondrial disorders v1.213 TRIT1 Sarah Leigh Phenotypes for gene: TRIT1 were changed from No OMIM phenotype; Multiple respiratory chain complex deficiencies (disorders of protein synthesis) to Combined oxidative phosphorylation deficiency 35 617873
Mitochondrial disorders TRIT1 Zornitza Stark reviewed gene: TRIT1