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Acute rhabdomyolysis v1.21 PHKB Arina Puzriakova Tag Q3_23_expert_review was removed from gene: PHKB.
Tag Q3_23_demote_red was removed from gene: PHKB.
Acute rhabdomyolysis v1.21 PHKB Arina Puzriakova edited their review of gene: PHKB: Added comment: The rating of this gene has been updated to Red following NHS Genomic Medicine Service approval. Additional comments from reviewing GLHs: NW: In keeping with previous NHS GMS review for equivalent panel. NEY: PHKB which has never had an association with Rhabdomyolysis and so I agree with its removal from the panel.; Changed rating: RED
Acute rhabdomyolysis v1.20 PHKB Arina Puzriakova Source Expert Review Red was added to PHKB.
Rating Changed from Green List (high evidence) to Red List (low evidence)
Acute rhabdomyolysis v1.13 PHKB Achchuthan Shanmugasundram Classified gene: PHKB as Green List (high evidence)
Acute rhabdomyolysis v1.13 PHKB Achchuthan Shanmugasundram Added comment: Comment on list classification: PHKB gene was demoted to Red in 'Rhabdomyolysis and metabolic muscle disorders' panel (https://panelapp.genomicsengland.co.uk/panels/66/gene/PHKB/) in agreement with the NHS Genomic Medicine Service. Hence, we propose that this gene should be reviewed for demotion to red in this panel.
Acute rhabdomyolysis v1.13 PHKB Achchuthan Shanmugasundram Gene: phkb has been classified as Green List (High Evidence).
Acute rhabdomyolysis v1.12 PHKB Achchuthan Shanmugasundram Tag Q3_23_expert_review tag was added to gene: PHKB.
Tag Q3_23_demote_red tag was added to gene: PHKB.
Acute rhabdomyolysis v1.12 PHKB Achchuthan Shanmugasundram reviewed gene: PHKB: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: Phosphorylase kinase deficiency of liver and muscle, autosomal recessive, OMIM:261750; Mode of inheritance: None
Acute rhabdomyolysis v0.6 PHKB Arina Puzriakova reviewed gene: PHKB: Rating: GREEN; Mode of pathogenicity: ; Publications: ; Phenotypes: ; Mode of inheritance:
Acute rhabdomyolysis v0.2 PHKB Arina Puzriakova gene: PHKB was added
gene: PHKB was added to Acute rhabdomyolysis. Sources: Expert Review Green,NHS GMS
Mode of inheritance for gene: PHKB was set to BIALLELIC, autosomal or pseudoautosomal
Phenotypes for gene: PHKB were set to Phosphorylase kinase deficiency of liver and muscle, autosomal recessive, OMIM:261750