Details
| Type | Protein Coding |
| Official Symbol | DEAF1 |
| Official Name | DEAF1 transcription factor [Source:HGNC Symbol;Acc:HGNC:14677] |
| Ensembl ID | ENSG00000282712 |
| Bio databases IDs | |
| Aliases | DEAF1 transcription factor |
| Species | Human, Homo sapiens |
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- NEURODEVELOPMENTAL DISORDER WITH HYPOTONIA AND IMPAIRED EXPRESSIVE LANGUAGE AND WITH OR WITHOUT SEIZURES
- VULTO-VAN SILFHOUT-DE VRIES SYNDROME
- Autism intellectual disability basal ganglia dysfunction and epilepsy
- Mental retardation autosomal dominant 24