Gene
deaf1
- ID
- ZDB-GENE-081022-163
- Name
- DEAF1 transcription factor
- Symbol
- deaf1 Nomenclature History
- Previous Names
-
- zgc:194895
- Type
- protein_coding_gene
- Location
- Chr: 25 Mapping Details/Browsers
- Description
- Predicted to have DNA-binding transcription factor activity. Predicted to be involved in regulation of transcription by RNA polymerase II. Predicted to localize to nucleus. Human ortholog(s) of this gene implicated in autosomal dominant non-syndromic intellectual disability 24. Orthologous to human DEAF1 (DEAF1 transcription factor).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| Vulto-van Silfout-de Vries syndrome | Alliance | Vulto-van Silfout-de Vries syndrome | 615828 |
| Neurodevelopmental disorder with hypotonia, impaired expressive language, and with or without seizures | 617171 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | SAND domain | SAND-like domain superfamily | Zinc finger, MYND-type |
|---|---|---|---|---|
|
UniProtKB:A0A8M2BLH6
|
532 | |||
|
UniProtKB:B3DHN2
|
528 |
Interactions and Pathways
No data available
Plasmids
No data available