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Mitochondrial disorders v3.6 NDUFB10 Achchuthan Shanmugasundram Tag Q3_22_rating was removed from gene: NDUFB10.
Mitochondrial disorders v3.6 NDUFB10 Achchuthan Shanmugasundram reviewed gene: NDUFB10: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Mitochondrial disorders v3.5 NDUFB10 Achchuthan Shanmugasundram Source NHS GMS was added to NDUFB10.
Source Expert Review Green was added to NDUFB10.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v2.144 NDUFB10 Arina Puzriakova Classified gene: NDUFB10 as Amber List (moderate evidence)
Mitochondrial disorders v2.144 NDUFB10 Arina Puzriakova Gene: ndufb10 has been classified as Amber List (Moderate Evidence).
Mitochondrial disorders v2.143 NDUFB10 Arina Puzriakova Publications for gene: NDUFB10 were set to 28040730
Mitochondrial disorders v2.142 NDUFB10 Arina Puzriakova Phenotypes for gene: NDUFB10 were changed from Isolated complex I deficiency; No OMIM phenotype to Mitochondrial complex I deficiency, nuclear type 35, OMIM:619003
Mitochondrial disorders v2.123 NDUFB10 Arina Puzriakova reviewed gene: NDUFB10: Rating: GREEN; Mode of pathogenicity: ; Publications: 28040730, 32025618, 33169436; Phenotypes: Mitochondrial complex I deficiency, nuclear type 35, OMIM: 619003; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v2.122 NDUFB10 Arina Puzriakova Tag Q3_22_rating tag was added to gene: NDUFB10.
Mitochondrial disorders v2.12 NDUFB10 Zornitza Stark edited their review of gene: NDUFB10: Added comment: Second family reported, including more functional data.; Changed rating: GREEN; Changed publications: 28040730, 32025618, 33169436; Changed phenotypes: fatal infantile lactic acidosis, cardiomyopathy, Mitochondrial complex I deficiency nuclear type 35 (MC1DN35), MIM#619003
Mitochondrial disorders v2.5 NDUFB10 Zornitza Stark reviewed gene: NDUFB10: Rating: AMBER; Mode of pathogenicity: None; Publications: 28040730, 32025618; Phenotypes: fatal infantile lactic acidosis, cardiomyopathy; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v1.465 NDUFB10 Sarah Leigh Mode of inheritance for gene: NDUFB10 was changed from to BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v1.383 NDUFB10 Ellen McDonagh Publications for gene: NDUFB10 were set to
Mitochondrial disorders v1.292 NDUFB10 Sarah Leigh edited their review of gene: NDUFB10: Added comment: Two variants in a compound heterozygous case with fatal infantile lactic acidosis and cardiomyopathy. Supportive functional studies were also performed.; Changed rating: AMBER
Mitochondrial disorders v1.292 NDUFB10 Sarah Leigh reviewed gene: NDUFB10: Rating: ; Mode of pathogenicity: None; Publications: 28040730; Phenotypes: ; Mode of inheritance: None