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Genetic Epilepsy v2.0 GRIA4 Gene migrated from ENSG00000152578 to ENSG00000152578 (gene set migration)
Genetic Epilepsy v0.1603 GRIA4 Ain Roesley Phenotypes for gene: GRIA4 were changed from Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864 to Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864
Genetic Epilepsy v0.1603 GRIA4 Ain Roesley Phenotypes for gene: GRIA4 were changed from Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864 to Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864
Genetic Epilepsy v0.1603 GRIA4 Ain Roesley Publications for gene: GRIA4 were set to 35518358; 29220673
Genetic Epilepsy v0.1603 GRIA4 Ain Roesley Phenotypes for gene: GRIA4 were changed from Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864 to Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864
Genetic Epilepsy v0.1603 GRIA4 Ain Roesley Publications for gene: GRIA4 were set to 35518358; 29220673
Genetic Epilepsy v0.1603 GRIA4 Ain Roesley Phenotypes for gene: GRIA4 were changed from Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864 to Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864
Genetic Epilepsy v0.1602 GRIA4 Ain Roesley Phenotypes for gene: GRIA4 were changed from to Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864
Genetic Epilepsy v0.1602 GRIA4 Ain Roesley Publications for gene: GRIA4 were set to
Genetic Epilepsy v0.1602 GRIA4 Ain Roesley Marked gene: GRIA4 as ready
Genetic Epilepsy v0.1602 GRIA4 Ain Roesley Gene: gria4 has been classified as Green List (High Evidence).
Genetic Epilepsy v0.1602 GRIA4 Ain Roesley Mode of inheritance for gene: GRIA4 was changed from Unknown to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Genetic Epilepsy v0.1601 GRIA4 Ain Roesley reviewed gene: GRIA4: Rating: GREEN; Mode of pathogenicity: None; Publications: 35518358, 29220673; Phenotypes: Neurodevelopmental disorder with or without seizures and gait abnormalities MIM#617864; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted; Current diagnostic: yes
Genetic Epilepsy v0.0 GRIA4 Zornitza Stark gene: GRIA4 was added
gene: GRIA4 was added to Genetic Epilepsy_AustralianGenomics_VCGS. Sources: Australian Genomics Health Alliance Epilepsy Flagship,Expert Review Green,Victorian Clinical Genetics Services
Mode of inheritance for gene: GRIA4 was set to Unknown