Gene
oclna
- ID
- ZDB-GENE-040426-2685
- Name
- occludin a
- Symbol
- oclna Nomenclature History
- Previous Names
- Type
- protein_coding_gene
- Location
- Chr: 10 Mapping Details/Browsers
- Description
- Predicted to be involved in bicellular tight junction assembly. Predicted to localize to bicellular tight junction; integral component of membrane; and plasma 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; musculature system; pleuroperitoneal region; and sensory system. Orthologous to human OCLN (occludin).
- Genome Resources
- Note
- None
- Comparative Information
-
- All Expression Data
- 22 figures from 10 publications
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
-
- MGC:56359 (20 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 | Occludin homology domain |
|---|---|---|---|---|---|
|
UniProtKB:F1R799
|
491 |
Interactions and Pathways
No data available
Plasmids
No data available