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Carney complex v1.2 PRKAR1A Achchuthan Shanmugasundram Added comment: Comment on phenotypes: This gene has been associated with relevant phenotypes in OMIM (MIM #160980) and the OMIM record was last accessed on 17 December 2025.
Carney complex v1.2 PRKAR1A Achchuthan Shanmugasundram Phenotypes for gene: PRKAR1A were changed from to Carney complex, OMIM:160980; Carney complex, type 1, MONDO:0008057
Carney complex v1.1 Achchuthan Shanmugasundram Panel version 1.0 has been signed off on 2023-09-14
Carney complex v1.0 Achchuthan Shanmugasundram promoted panel to version 1.0
Carney complex v0.3 Achchuthan Shanmugasundram Panel types changed to GMS Rare Disease; GMS signed-off
Carney complex v0.2 Achchuthan Shanmugasundram Panel status changed from internal to public
Carney complex v0.1 PRKAR1A Achchuthan Shanmugasundram reviewed gene: PRKAR1A: Rating: GREEN; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Carney complex v0.1 PRKAR1A Achchuthan Shanmugasundram gene: PRKAR1A was added
gene: PRKAR1A was added to Carney complex. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: PRKAR1A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Carney complex v0.0 Achchuthan Shanmugasundram Added Panel Carney complex
Set list of related panels to R156
Set panel types to: GMS Rare Disease