Gene
wnt5b
- ID
- ZDB-GENE-980526-87
- Name
- wingless-type MMTV integration site family, member 5b
- Symbol
- wnt5b Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 4 Mapping Details/Browsers
- Description
- Exhibits signaling receptor binding activity. Involved in several processes, including animal organ development; convergent extension; and vasculature development. Predicted to localize to extracellular space. Human ortholog(s) of this gene implicated in autosomal dominant Robinow syndrome 1. Is expressed in several structures, including central nervous system; fin; germ ring; head; and mesoderm. Orthologous to several human genes including WNT5B (Wnt family member 5B).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 57 figures from 45 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- eu891 (17 images)
Wild Type Expression Summary
- All Phenotype Data
- 80 figures from 37 publications
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Wnt | Wnt, C-terminal domain | Wnt protein, conserved site |
|---|---|---|---|---|
|
UniProtKB:Q92050
|
363 | |||
|
UniProtKB:A0A8M6Z5V6
|
380 | |||
|
UniProtKB:B3DI33
|
363 |
Interactions and Pathways
No data available
Plasmids