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Cerebral Palsy v1.194 TUBB2B Clare van Eyk reviewed gene: TUBB2B: Rating: GREEN; Mode of pathogenicity: None; Publications: PMID: 38693247; Phenotypes: Cortical dysplasia, complex, with other brain malformations 7, MIM#610031; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cerebral Palsy v1.88 TUBB2B Zornitza Stark Marked gene: TUBB2B as ready
Cerebral Palsy v1.88 TUBB2B Zornitza Stark Gene: tubb2b has been classified as Green List (High Evidence).
Cerebral Palsy v1.88 TUBB2B Zornitza Stark Publications for gene: TUBB2B were set to PMID: 33528536
Cerebral Palsy v1.87 TUBB2B Zornitza Stark Classified gene: TUBB2B as Green List (high evidence)
Cerebral Palsy v1.87 TUBB2B Zornitza Stark Gene: tubb2b has been classified as Green List (High Evidence).
Cerebral Palsy v1.86 TUBB2B Luisa Weiss reviewed gene: TUBB2B: Rating: GREEN; Mode of pathogenicity: None; Publications: 33528536, 34077496; Phenotypes: Cortical dysplasia, complex, with other brain malformations MIM#610031; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cerebral Palsy v1.11 TUBB2B Zornitza Stark Marked gene: TUBB2B as ready
Cerebral Palsy v1.11 TUBB2B Zornitza Stark Gene: tubb2b has been classified as Red List (Low Evidence).
Cerebral Palsy v1.6 TUBB2B Chirag Patel reviewed gene: TUBB2B: Rating: RED; Mode of pathogenicity: None; Publications: ; Phenotypes: ; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Cerebral Palsy v1.3 TUBB2B Chirag Patel Deleted their review
Cerebral Palsy v1.3 TUBB2B Chirag Patel gene: TUBB2B was added
gene: TUBB2B was added to Cerebral Palsy. Sources: Literature
Mode of inheritance for gene: TUBB2B was set to MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted
Publications for gene: TUBB2B were set to PMID: 33528536
Phenotypes for gene: TUBB2B were set to Cortical dysplasia, complex, with other brain malformations 7, OMIM # 610031
Review for gene: TUBB2B was set to RED
Added comment: Moreno-De-Luca et al. (2021) reported 3 patients with cerebral palsy with de novo pathogenic/LP variants BUT primarily presents with cortical malformations
Sources: Literature