Gene
washc5
- ID
- ZDB-GENE-040426-838
- Name
- WASH complex subunit 5
- Symbol
- washc5 Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 16 Mapping Details/Browsers
- Description
- Involved in axonogenesis and heart contraction. Predicted to localize to WASH complex. Human ortholog(s) of this gene implicated in Ritscher-Schinzel syndrome 1 and hereditary spastic paraplegia 8. Orthologous to human WASHC5 (WASH complex subunit 5).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 1 figure from Bu et al., 2020
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
Phenotype Summary
Mutations
Human Disease
| Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
|---|---|---|---|
| hereditary spastic paraplegia 8 | Alliance | Spastic paraplegia 8, autosomal dominant | 603563 |
| Ritscher-Schinzel syndrome 1 | Alliance | Ritscher-Schinzel syndrome 1 | 220210 |
Domain, Family, and Site Summary
| Type | InterPro ID | Name |
|---|---|---|
| Family | IPR019393 | WASH complex, subunit strumpellin |
Domain Details Per Protein
| Protein | Length | WASH complex, subunit strumpellin |
|---|---|---|
|
UniProtKB:Q7ZVM1
|
1159 |
| Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
|---|---|---|---|---|---|
| mRNA |
washc5-201
(1)
|
Ensembl | 3,228 nt |
Interactions and Pathways
No data available
Plasmids
No data available