Details
| Type | Protein Coding |
| Official Symbol | OCLN |
| Official Name | occludin [Source:HGNC Symbol;Acc:HGNC:8104] |
| Ensembl ID | ENSG00000273814 |
| Bio databases IDs | |
| Aliases | occludin |
| Species | Human, Homo sapiens |
Pathways
Biological processes and signaling networks where the OCLN gene in human plays a role, providing insight into its function and relevance in health or disease.
Top Findings
The most significant associations for this gene, including commonly observed domains, pathway involvement, and functional highlights based on current data.
phenotypes
- PSEUDO-TORCH SYNDROME 1
- OCLN-associated Band-like Calcification with Simplified Gyration and Polymicrogyria