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Genetic Epilepsy v0.1944 COG3 Zornitza Stark Phenotypes for gene: COG3 were changed from Neurodevelopmental disorder (MONDO#0700092), COG3-related to Congenital disorder of glycosylation, type IIbb, MIM# 620546
Genetic Epilepsy v0.1943 COG3 Zornitza Stark reviewed gene: COG3: Rating: AMBER; Mode of pathogenicity: None; Publications: ; Phenotypes: Congenital disorder of glycosylation, type IIbb, MIM# 620546; Mode of inheritance: BIALLELIC, autosomal or pseudoautosomal
Genetic Epilepsy v0.1931 COG3 Elena Savva Classified gene: COG3 as Amber List (moderate evidence)
Genetic Epilepsy v0.1931 COG3 Elena Savva Gene: cog3 has been classified as Amber List (Moderate Evidence).
Genetic Epilepsy v0.1931 COG3 Elena Savva Classified gene: COG3 as Amber List (moderate evidence)
Genetic Epilepsy v0.1931 COG3 Elena Savva Gene: cog3 has been classified as Amber List (Moderate Evidence).
Genetic Epilepsy v0.1931 COG3 Elena Savva Classified gene: COG3 as Amber List (moderate evidence)
Genetic Epilepsy v0.1931 COG3 Elena Savva Gene: cog3 has been classified as Amber List (Moderate Evidence).
Genetic Epilepsy v0.1930 COG3 Elena Savva Marked gene: COG3 as ready
Genetic Epilepsy v0.1930 COG3 Elena Savva Gene: cog3 has been removed from the panel.
Genetic Epilepsy v0.1927 COG3 Daniel Flanagan gene: COG3 was added
gene: COG3 was added to Genetic Epilepsy. Sources: Expert list
Mode of inheritance for gene: COG3 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: COG3 were set to PMID: 37711075
Phenotypes for gene: COG3 were set to Neurodevelopmental disorder (MONDO#0700092), COG3-related
Review for gene: COG3 was set to AMBER
Added comment: Two COG3 homozygous missense variants in four individuals from two unrelated consanguineous families. Clinical phenotypes of affected individuals include global developmental delay, severe intellectual disability, microcephaly, epilepsy, facial dysmorphism, and variable neurological findings.
Sources: Expert list