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Progressive Myoclonic Epilepsy v1.0 DNAJC5 Gene migrated from ENSG00000101152 to ENSG00000101152 (gene set migration)
Progressive Myoclonic Epilepsy v0.22 DNAJC5 Chirag Patel Source Royal Melbourne Hospital was removed from DNAJC5.
Source Expert list was added to DNAJC5.
Phenotypes for gene: DNAJC5 were changed from autosomal dominant Kufs disease; generalized tonic clonic seizures; Ceroid lipofuscinosis, neuronal, 4, Parry type, 162350 to Ceroid lipofuscinosis, neuronal, 4 (Kufs type), MONDO:0008083
Progressive Myoclonic Epilepsy v0.13 DNAJC5 Bryony Thompson Marked gene: DNAJC5 as ready
Progressive Myoclonic Epilepsy v0.13 DNAJC5 Bryony Thompson Gene: dnajc5 has been classified as Green List (High Evidence).
Progressive Myoclonic Epilepsy v0.13 DNAJC5 Bryony Thompson Classified gene: DNAJC5 as Green List (high evidence)
Progressive Myoclonic Epilepsy v0.13 DNAJC5 Bryony Thompson Added comment: Comment on list classification: ClinGen Epilepsy GCEP gene-disease curation: Moderate, >3 families reported. Classification - 07/30/2021
Progressive Myoclonic Epilepsy v0.13 DNAJC5 Bryony Thompson Gene: dnajc5 has been classified as Green List (High Evidence).
Progressive Myoclonic Epilepsy v0.12 DNAJC5 Bryony Thompson Publications for gene: DNAJC5 were set to
Progressive Myoclonic Epilepsy v0.0 DNAJC5 Bryony Thompson gene: DNAJC5 was added
gene: DNAJC5 was added to Progressive Myoclonic Epilepsy_RMH. Sources: Expert Review Green,Royal Melbourne Hospital
Mode of inheritance for gene: DNAJC5 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
Phenotypes for gene: DNAJC5 were set to autosomal dominant Kufs disease; generalized tonic clonic seizures; Ceroid lipofuscinosis, neuronal, 4, Parry type, 162350