Gene
brwd3
- ID
- ZDB-GENE-100921-43
- Name
- bromodomain and WD repeat domain containing 3
- Symbol
- brwd3 Nomenclature History
- Previous Names
-
- si:dkey-237j10.3
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Predicted to be involved in cytoskeleton organization; regulation of cell shape; and regulation of transcription by RNA polymerase II. Predicted to localize to nucleus. Human ortholog(s) of this gene implicated in non-syndromic X-linked intellectual disability. Orthologous to human BRWD3 (bromodomain and WD repeat domain containing 3).
- 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 |
---|---|---|---|
non-syndromic X-linked intellectual disability 93 | Alliance | Intellectual developmental disorder, X-linked 93 | 300659 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Protein | Length |
---|---|
UniProtKB:A0A8M3B2F0
|
1741 |
UniProtKB:A0A8M9Q1J4
|
1740 |
UniProtKB:A0A8M3ASD3
|
1742 |
UniProtKB:A0A8M9PQW9
|
1741 |
Interactions and Pathways
No data available
Plasmids
No data available