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Mitochondrial disorders v3.6 LYRM4 Achchuthan Shanmugasundram Tag Q3_22_rating was removed from gene: LYRM4.
Mitochondrial disorders v3.6 LYRM4 Achchuthan Shanmugasundram reviewed gene: LYRM4: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Mitochondrial disorders v3.5 LYRM4 Achchuthan Shanmugasundram Source NHS GMS was added to LYRM4.
Source Expert Review Green was added to LYRM4.
Rating Changed from Amber List (moderate evidence) to Green List (high evidence)
Mitochondrial disorders v2.132 LYRM4 Arina Puzriakova Classified gene: LYRM4 as Amber List (moderate evidence)
Mitochondrial disorders v2.132 LYRM4 Arina Puzriakova Gene: lyrm4 has been classified as Amber List (Moderate Evidence).
Mitochondrial disorders v2.131 LYRM4 Arina Puzriakova Phenotypes for gene: LYRM4 were changed from ?Combined oxidative phosphorylation deficiency 19, 615595 to Combined oxidative phosphorylation deficiency 19, OMIM:615595
Mitochondrial disorders v2.130 LYRM4 Arina Puzriakova Publications for gene: LYRM4 were set to
Mitochondrial disorders v2.123 LYRM4 Arina Puzriakova reviewed gene: LYRM4: Rating: GREEN; Mode of pathogenicity: ; Publications: 31497476, 23814038; Phenotypes: Combined oxidative phosphorylation deficiency 19, OMIM: 615595; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v2.122 LYRM4 Arina Puzriakova Tag Q3_22_rating tag was added to gene: LYRM4.
Mitochondrial disorders v2.5 LYRM4 Zornitza Stark changed review comment from: Three individuals from two families reported.; to: Three individuals from two families reported. Amber on the other mito panel.
Mitochondrial disorders v2.5 LYRM4 Zornitza Stark reviewed gene: LYRM4: Rating: AMBER; Mode of pathogenicity: None; Publications: 23814038, 31497476; Phenotypes: Combined oxidative phosphorylation deficiency 19, MIM# 615595; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Mitochondrial disorders v1.467 LYRM4 Sarah Leigh Mode of inheritance for gene: LYRM4 was changed from to BIALLELIC, autosomal or pseudoautosomal