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Date	Panel	Item	Activity
Filter activities 12 actions
07 Jun 2026	Mitochondrial disease v2.0	CLPB	Gene migrated from ENSG00000162129 to ENSG00000162129 (gene set migration)
20 Apr 2022	Mitochondrial disease v0.789	CLPB	Zornitza Stark Phenotypes for gene: CLPB were changed from 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropaenia, MIM# 616271; Neutropenia, severe congenital, 9, autosomal dominant, MIM# 619813 to 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropaenia, MIM# 616271; 3-methylglutaconic aciduria, type VIIA, autosomal dominant, MIM# 619835; Neutropenia, severe congenital, 9, autosomal dominant, MIM# 619813
20 Apr 2022	Mitochondrial disease v0.788	CLPB	Zornitza Stark edited their review of gene: CLPB: Changed phenotypes: 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropaenia, MIM# 616271, 3-methylglutaconic aciduria, type VIIA, autosomal dominant, MIM# 619835, Neutropenia, severe congenital, 9, autosomal dominant, MIM# 619813
15 Apr 2022	Mitochondrial disease v0.788	CLPB	Zornitza Stark Phenotypes for gene: CLPB were changed from 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropaenia, MIM# 616271 to 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropaenia, MIM# 616271; Neutropenia, severe congenital, 9, autosomal dominant, MIM# 619813
15 Apr 2022	Mitochondrial disease v0.787	CLPB	Zornitza Stark edited their review of gene: CLPB: Changed phenotypes: 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropaenia, MIM# 616271, Neutropenia, severe congenital, 9, autosomal dominant, MIM# 619813
23 Jun 2021	Mitochondrial disease v0.636	CLPB	Zornitza Stark Marked gene: CLPB as ready
23 Jun 2021	Mitochondrial disease v0.636	CLPB	Zornitza Stark Gene: clpb has been classified as Green List (High Evidence).
23 Jun 2021	Mitochondrial disease v0.636	CLPB	Zornitza Stark Phenotypes for gene: CLPB were changed from to 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropaenia, MIM# 616271
23 Jun 2021	Mitochondrial disease v0.635	CLPB	Zornitza Stark Publications for gene: CLPB were set to
23 Jun 2021	Mitochondrial disease v0.634	CLPB	Zornitza Stark Mode of inheritance for gene: CLPB was changed from Unknown to BOTH monoallelic and biallelic, autosomal or pseudoautosomal
23 Jun 2021	Mitochondrial disease v0.633	CLPB	Zornitza Stark reviewed gene: CLPB: Rating: GREEN; Mode of pathogenicity: None; Publications: 25597510, 34140661; Phenotypes: 3-methylglutaconic aciduria, type VII, with cataracts, neurologic involvement and neutropaenia, MIM# 616271; Mode of inheritance: BOTH monoallelic and biallelic, autosomal or pseudoautosomal
18 Nov 2019	Mitochondrial disease v0.0	CLPB	Zornitza Stark gene: CLPB was added gene: CLPB was added to Mitochondrial_AGHA_VCGS. Sources: Expert Review Green,Australian Genomics Health Alliance Mitochondrial Flagship,Victorian Clinical Genetics Services Mode of inheritance for gene: CLPB was set to Unknown