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Retinoblastoma v1.2 RB1 Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #180200) and the OMIM record was last accessed on 29 December 2025.
Retinoblastoma v1.2 RB1 Achchuthan Shanmugasundram Phenotypes for gene: RB1 were changed from to Retinoblastoma, OMIM:180200; Retinoblastoma, trilateral, OMIM:180200; hereditary retinoblastoma, MONDO:0018160
Retinoblastoma v1.1 Mafalda Gomes Panel version 1.0 has been signed off on 2023-09-14
Retinoblastoma v1.0 Mafalda Gomes promoted panel to version 1.0
Retinoblastoma v0.3 Mafalda Gomes Panel types changed to GMS Rare Disease; GMS signed-off
Retinoblastoma v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Retinoblastoma v0.1 RB1 Achchuthan Shanmugasundram reviewed gene: RB1: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Retinoblastoma v0.1 RB1 Achchuthan Shanmugasundram gene: RB1 was added
gene: RB1 was added to Retinoblastoma. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: RB1 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Retinoblastoma v0.0 Achchuthan Shanmugasundram Added Panel Retinoblastoma
Set list of related panels to R219
Set panel types to: GMS Rare Disease