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Cerebral Palsy v2.0 TUBB4A Gene migrated from ENSG00000104833 to ENSG00000104833 (gene set migration)
Cerebral Palsy v1.213 TUBB4A Zornitza Stark Publications for gene: TUBB4A were set to 34531397; 33528536
Cerebral Palsy v1.194 TUBB4A Clare van Eyk reviewed gene: TUBB4A: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 38693247; Phenotypes: Dystonia 4, torsion, autosomal dominant, MIM#128101, Leukodystrophy, hypomyelinating, 6, MIM#612438; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cerebral Palsy v1.12 TUBB4A Zornitza Stark Marked gene: TUBB4A as ready
Cerebral Palsy v1.12 TUBB4A Zornitza Stark Gene: tubb4a has been classified as Green List (High Evidence).
Cerebral Palsy v1.12 TUBB4A Zornitza Stark Publications for gene: TUBB4A were set to PMID: 34531397, 33528536
Cerebral Palsy v1.6 TUBB4A chirag patel Classified gene: TUBB4A as Green List (high evidence)
Cerebral Palsy v1.6 TUBB4A chirag patel Gene: tubb4a has been classified as Green List (High Evidence).
Cerebral Palsy v1.5 TUBB4A chirag patel Classified gene: TUBB4A as Green List (high evidence)
Cerebral Palsy v1.5 TUBB4A chirag patel Gene: tubb4a has been classified as Green List (High Evidence).
Cerebral Palsy v1.5 TUBB4A chirag patel Classified gene: TUBB4A as Green List (high evidence)
Cerebral Palsy v1.5 TUBB4A chirag patel Gene: tubb4a has been classified as Green List (High Evidence).
Cerebral Palsy v1.4 TUBB4A chirag patel gene: TUBB4A was added
gene: TUBB4A was added to Cerebral Palsy. Sources: Literature
Mode of inheritance for gene: TUBB4A was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TUBB4A were set to PMID: 34531397, 33528536
Phenotypes for gene: TUBB4A were set to Dystonia 4, torsion, autosomal dominant, OMIM #128101; Leukodystrophy, hypomyelinating, 6, OMIM # 612438
Review for gene: TUBB4A was set to GREEN
Added comment: Van Eyk et al. (2021) reported 1 patient with dystonic CP with de novo variant. Moreno-De-Luca et al. (2021) reported 6 patients with CP with P/LP variants.
Sources: Literature