Gene
wt1b
- ID
- ZDB-GENE-050420-319
- Name
- WT1 transcription factor b
- Symbol
- wt1b Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 18 Mapping Details/Browsers
- Description
- Predicted to have DNA-binding transcription factor activity, RNA polymerase II-specific. Involved in glomerular visceral epithelial cell differentiation and pronephros development. Predicted to localize to nucleus. Human ortholog(s) of this gene implicated in several diseases, including Denys-Drash syndrome; Frasier syndrome; malignant mesothelioma; nephroblastoma; and nephrotic syndrome type 4. Is expressed in several structures, including eye; heart; intermediate mesoderm; pleuroperitoneal region; and podocyte. Orthologous to human WT1 (WT1 transcription factor).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 39 figures from 18 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 |
|---|---|---|---|
| Denys-Drash syndrome | Alliance | Denys-Drash syndrome | 194080 |
| Frasier syndrome | Alliance | Frasier syndrome | 136680 |
| malignant mesothelioma | Alliance | Mesothelioma, somatic | 156240 |
| nephroblastoma | Alliance | Wilms tumor, type 1 | 194070 |
| nephrotic syndrome type 4 | Alliance | Nephrotic syndrome, type 4 | 256370 |
| Meacham syndrome | 608978 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | Wilm's tumour protein, N-terminal | Zinc finger C2H2 superfamily | Zinc finger C2H2-type |
|---|---|---|---|---|
|
UniProtKB:Q08CU4
|
404 | |||
|
UniProtKB:A0A8M2B680
|
409 |
Interactions and Pathways
No data available
Plasmids