Gene
wnt2ba
- ID
- ZDB-GENE-030717-2
- Name
- wingless-type MMTV integration site family, member 2Ba
- Symbol
- wnt2ba Nomenclature History
- Previous Names
-
- wnt2b
- Type
- protein_coding_gene
- Location
- Chr: 6 Mapping Details/Browsers
- Description
- Predicted to have frizzled binding activity. Involved in embryonic pectoral fin morphogenesis and sensory epithelium regeneration. Predicted to localize to extracellular space. Human ortholog(s) of this gene implicated in congenital diarrhea. Is expressed in brain; immature eye; intermediate mesoderm; pectoral fin field; and pronephros. Orthologous to human WNT2B (Wnt family member 2B).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 11 figures from 8 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 |
|---|---|---|---|
| Diarrhea 9 | 618168 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Wnt | Wnt-2 protein | Wnt, C-terminal domain | Wnt protein, conserved site |
|---|---|---|---|---|---|
|
UniProtKB:Q8AY89
|
387 | ||||
|
UniProtKB:A0A8M3B3N2
|
230 |
| Type | Name | Annotation Method | Length (nt) | Analysis |
|---|---|---|---|---|
| mRNA |
wnt2ba-201
(1)
|
Havana | 1771 nt |
Interactions and Pathways
No data available
Plasmids
No data available