Gene
wnt7ab
- ID
- ZDB-GENE-100922-44
- Name
- wingless-type MMTV integration site family, member 7Ab
- Symbol
- wnt7ab Nomenclature History
- Previous Names
- None
- Type
- protein_coding_gene
- Location
- Unmapped
- Description
- Predicted to have signaling receptor binding activity. Predicted to be involved in Wnt signaling pathway and multicellular organism development. Predicted to localize to extracellular region. Is expressed in hindbrain and hindbrain neural keel.
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 2 figures from Beretta et al., 2011
- 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 |
|---|---|---|---|
| Fuhrmann syndrome | Alliance | Fuhrmann syndrome | 228930 |
| Schinzel type phocomelia | Alliance | Ulna and fibula, absence of, with severe limb deficiency | 276820 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Wnt | Wnt-7 protein | Wnt, C-terminal domain | Wnt protein, conserved site |
|---|---|---|---|---|---|
|
UniProtKB:E7FBM9
|
- Genome Browsers
- No data available
Interactions and Pathways
No data available
Plasmids
No data available