Gene
wnt5a
- ID
- ZDB-GENE-060328-3
- Name
- wingless-type MMTV integration site family, member 5a
- Symbol
- wnt5a Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Chr: 8 Mapping Details/Browsers
- Description
- Predicted to have frizzled binding activity. Involved in pronephros development. Predicted to localize to extracellular space. Human ortholog(s) of this gene implicated in autosomal dominant Robinow syndrome 1. Is expressed in brain; neural crest cell; ovarian follicle; pronephros; and tooth placode. Orthologous to human WNT5A (Wnt family member 5A).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 13 figures from 13 publications
- 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 |
|---|---|---|---|
| autosomal dominant Robinow syndrome 1 | Alliance | Robinow syndrome, autosomal dominant 1 | 180700 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Wnt | Wnt, C-terminal domain | Wnt protein, conserved site |
|---|---|---|---|---|
|
UniProtKB:A1BPR0
|
374 |
- Genome Browsers
Interactions and Pathways
No data available
Plasmids
No data available