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Optic Atrophy v1.26 MECR Zornitza Stark Phenotypes for gene: MECR were changed from Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities to Optic atrophy 16, MIM# 620629
Optic Atrophy v1.25 MECR Zornitza Stark reviewed gene: MECR: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: Optic atrophy 16, MIM# 620629; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Optic Atrophy v0.32 MECR Zornitza Stark Marked gene: MECR as ready
Optic Atrophy v0.32 MECR Zornitza Stark Gene: mecr has been classified as Green List (High Evidence).
Optic Atrophy v0.26 MECR Zornitza Stark Phenotypes for gene: MECR were changed from Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities to Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
Optic Atrophy v0.22 MECR Zornitza Stark Phenotypes for gene: MECR were changed from to Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities
Optic Atrophy v0.17 MECR Zornitza Stark Publications for gene: MECR were set to
Optic Atrophy v0.16 MECR Zornitza Stark Mode of inheritance for gene: MECR was changed from Unknown to BIALLELIC, autosomal or pseudoautosomal
Optic Atrophy v0.11 MECR Elena Savva reviewed gene: MECR: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 27817865, 31137067; Phenotypes: Dystonia, childhood-onset, with optic atrophy and basal ganglia abnormalities; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Optic Atrophy v0.0 MECR Zornitza Stark gene: MECR was added
gene: MECR was added to Optic Atrophy_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: MECR was set to Unknown