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Early onset or syndromic epilepsy v1.360 CCND2 Rebecca Foulger Marked gene: CCND2 as ready
Early onset or syndromic epilepsy v1.360 CCND2 Rebecca Foulger Gene: ccnd2 has been classified as Red List (Low Evidence).
Early onset or syndromic epilepsy v1.360 CCND2 Rebecca Foulger Classified gene: CCND2 as Red List (low evidence)
Early onset or syndromic epilepsy v1.360 CCND2 Rebecca Foulger Added comment: Comment on list classification: Demoted CCND2 from Amber to Red following Red reviews by Zornitza Stark and Tracy Lester- as noted previously by Sarah Leigh: epilepsy is not a reported feature of the disorder.
Early onset or syndromic epilepsy v1.360 CCND2 Rebecca Foulger Gene: ccnd2 has been classified as Red List (Low Evidence).
Early onset or syndromic epilepsy v1.359 CCND2 Rebecca Foulger Mode of inheritance for gene: CCND2 was changed from to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v1.358 CCND2 Rebecca Foulger Publications for gene: CCND2 were set to
Early onset or syndromic epilepsy v1.357 CCND2 Rebecca Foulger Phenotypes for gene: CCND2 were changed from to Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3, 615938
Early onset or syndromic epilepsy v1.191 CCND2 Rebecca Foulger Source Wessex and West Midlands GLH was added to CCND2.
Early onset or syndromic epilepsy v1.190 CCND2 Rebecca Foulger Source NHS GMS was added to CCND2.
Early onset or syndromic epilepsy v1.189 CCND2 Rebecca Foulger reviewed gene: CCND2: Rating: AMBER; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Early onset or syndromic epilepsy v1.188 CCND2 Tracy Lester reviewed gene: CCND2: Rating: RED; Mode of pathogenicity: ; Publications: 24705253; Phenotypes: Megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome 3, 615938; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Early onset or syndromic epilepsy v0.499 CCND2 Sarah Leigh Marked gene: CCND2 as ready
Early onset or syndromic epilepsy v0.499 CCND2 Sarah Leigh Added comment: Comment when marking as ready: Phenotype does not include seizures and to this gene is not relevant to the Genetic epilepsy syndromes panel.
Early onset or syndromic epilepsy v0.499 CCND2 Sarah Leigh Gene: ccnd2 has been classified as Amber List (Moderate Evidence).
Early onset or syndromic epilepsy CCND2 Zornitza Stark reviewed gene: CCND2
Early onset or syndromic epilepsy CCND2 Sarah Leigh Added gene to panel