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Genetic Epilepsy v0.1608 PCDHGC4 Zornitza Stark Phenotypes for gene: PCDHGC4 were changed from Neurodevelopmental disorder with poor growth and skeletal anomalies, MIM# 619880 to Neurodevelopmental disorder with poor growth and skeletal anomalies, MIM# 619880
Genetic Epilepsy v0.1607 PCDHGC4 Zornitza Stark Phenotypes for gene: PCDHGC4 were changed from Intellectual disability; Seizures to Neurodevelopmental disorder with poor growth and skeletal anomalies, MIM# 619880
Genetic Epilepsy v0.1606 PCDHGC4 Zornitza Stark edited their review of gene: PCDHGC4: Changed phenotypes: Neurodevelopmental disorder with poor growth and skeletal anomalies, MIM# 619880
Genetic Epilepsy v0.1144 PCDHGC4 Zornitza Stark Classified gene: PCDHGC4 as Green List (high evidence)
Genetic Epilepsy v0.1144 PCDHGC4 Zornitza Stark Gene: pcdhgc4 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.1143 PCDHGC4 Zornitza Stark Classified gene: PCDHGC4 as Green List (high evidence)
Genetic Epilepsy v0.1143 PCDHGC4 Zornitza Stark Gene: pcdhgc4 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.1142 PCDHGC4 Zornitza Stark Marked gene: PCDHGC4 as ready
Genetic Epilepsy v0.1142 PCDHGC4 Zornitza Stark Gene: pcdhgc4 has been classified as Red List (Low Evidence).
Genetic Epilepsy v0.1142 PCDHGC4 Zornitza Stark gene: PCDHGC4 was added
gene: PCDHGC4 was added to Genetic Epilepsy. Sources: Literature
Mode of inheritance for gene: PCDHGC4 was set to BIALLELIC, autosomal or pseudoautosomal
Publications for gene: PCDHGC4 were set to 34244665
Phenotypes for gene: PCDHGC4 were set to Intellectual disability; Seizures
Review for gene: PCDHGC4 was set to GREEN
Added comment: Eight variants reported in 19 members of nine unreleted families with a neurodevelopmental syndrome. Severe or moderate intellectual disabilty in eight families and seizures in four families. Four of the variants were LoF, in silico analysis of the remaining missense (n=3) and splice variants were predicted to be pathogenic.
Sources: Literature