Gene
oclnb
- ID
- ZDB-GENE-041212-43
- Name
- occludin b
- Symbol
- oclnb Nomenclature History
- Previous Names
-
- wu:fk83f10
- zgc:101820
- Type
- protein_coding_gene
- Location
- Chr: 5 Mapping Details/Browsers
- Description
- Predicted to localize to integral component of membrane. Human ortholog(s) of this gene implicated in Crohn's disease and pseudo-TORCH syndrome 1. Is expressed in several structures, including EVL; digestive system; extension; pleuroperitoneal region; and sensory system. Orthologous to human OCLN (occludin).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 17 figures from 7 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:101820 (12 images)
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 |
|---|---|---|---|
| pseudo-TORCH syndrome 1 | Alliance | Pseudo-TORCH syndrome 1 | 251290 |
Domain, Family, and Site Summary
Domain Details Per Protein
| Protein | Length | ELL/occludin family | Marvel domain | Occludin homology domain |
|---|---|---|---|---|
|
UniProtKB:Q5PRA1
|
461 | |||
|
UniProtKB:A2BGQ3
|
471 |
Interactions and Pathways
No data available
Plasmids
No data available