Gene
chd5
- ID
- ZDB-GENE-120314-2
- Name
- chromodomain helicase DNA binding protein 5
- Symbol
- chd5 Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 11 Mapping Details/Browsers
- Description
- Predicted to have ATP binding activity and metal ion binding activity. Involved in ATP-dependent chromatin remodeling; embryonic viscerocranium morphogenesis; and head development. Predicted to localize to integral component of membrane and nucleus. Is expressed in brain; eye; and testis. Orthologous to human CHD5 (chromodomain helicase DNA binding protein 5).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- 2 figures from Bishop et al., 2015
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- 6 figures from Bishop et al., 2015
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
Parenti-Mignot neurodevelopmental syndrome | 619873 |
Domain, Family, and Site Summary
No data available
Domain Details Per Protein
Protein | Length |
---|---|
UniProtKB:A0A8M3AXS2
|
2024 |
UniProtKB:A0A8M1RSV6
|
1996 |
UniProtKB:A0A8M9QI56
|
1995 |
UniProtKB:A0A8M3BDR6
|
2008 |
Interactions and Pathways
No data available
Plasmids
No data available