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Mendeliome v0.140 ERMARD Zornitza Stark Marked gene: ERMARD as ready
Mendeliome v0.140 ERMARD Zornitza Stark Added comment: Comment when marking as ready: Single affected individual described in heterozygous missense in this gene; rest of evidence is based on cytogenetic data.
Mendeliome v0.140 ERMARD Zornitza Stark Gene: ermard has been classified as Red List (Low Evidence).
Mendeliome v0.140 ERMARD Zornitza Stark Phenotypes for gene: ERMARD were changed from to Periventricular nodular heterotopia 6, MIM#615544
Mendeliome v0.139 ERMARD Zornitza Stark Publications for gene: ERMARD were set to
Mendeliome v0.138 ERMARD Zornitza Stark Mode of inheritance for gene: ERMARD was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.137 ERMARD Zornitza Stark Classified gene: ERMARD as Red List (low evidence)
Mendeliome v0.137 ERMARD Zornitza Stark Gene: ermard has been classified as Red List (Low Evidence).
Mendeliome v0.136 ERMARD Zornitza Stark reviewed gene: ERMARD: Rating: RED; Mode of pathogenicity: None; Publications: 24056535, 27087860; Phenotypes: Periventricular nodular heterotopia 6, MIM#615544; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Mendeliome v0.0 ERMARD Zornitza Stark gene: ERMARD was added
gene: ERMARD was added to Mendeliome_VCGS. Sources: Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: ERMARD was set to Unknown