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DDG2P v3.83 | BRD4 | Arina Puzriakova Added comment: Comment on phenotypes: Gene-checked tag removed as this gene now has a phenotype listed in OMIM (Cornelia de Lange syndrome 6, OMIM:620568) | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DDG2P v3.83 | BRD4 | Arina Puzriakova Phenotypes for gene: BRD4 were changed from CORNELIA DE LANGE-LIKE SYNDROME to Cornelia de Lange syndrome 6, OMIM:620568 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DDG2P v3.82 | BRD4 | Arina Puzriakova Tag gene-checked was removed from gene: BRD4. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DDG2P v3.73 | BRD4 | Eleanor Williams Tag gene-checked tag was added to gene: BRD4. | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DDG2P v3.73 | BRD4 | Eleanor Williams commented on gene: BRD4 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DDG2P v3.12 | BRD4 | Achchuthan Shanmugasundram reviewed gene: BRD4: Rating: GREEN; Mode of pathogenicity: ; Publications: 30302754, 29379197; Phenotypes: CORNELIA DE LANGE-LIKE SYNDROME; Mode of inheritance: MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DDG2P v3.11 | BRD4 |
Achchuthan Shanmugasundram Source Expert Review Green was added to BRD4. Publications for gene: BRD4 were updated from 29379197; 30302754 to 30302754; 29379197 Rating Changed from Amber List (moderate evidence) to Green List (high evidence) |
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DDG2P v1.74 | BRD4 | Rebecca Foulger commented on gene: BRD4 | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
DDG2P v1.73 | BRD4 |
Rebecca Foulger gene: BRD4 was added gene: BRD4 was added to DDG2P. Sources: DD-Gene2Phenotype,Expert Review Amber Mode of inheritance for gene: BRD4 was set to MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown Publications for gene: BRD4 were set to 29379197; 30302754 Phenotypes for gene: BRD4 were set to CORNELIA DE LANGE-LIKE SYNDROME |