Details
| Type | Retained Intron |
| Official Symbol | TINF2 |
| Official Name | TERF1 interacting nuclear factor 2 [Source:HGNC Symbol;Acc:HGNC:11824] |
| Ensembl ID | ENSG00000284915 |
| Bio databases IDs | |
| Aliases | TERF1 interacting nuclear factor 2 |
| Species | Human, Homo sapiens |
Pathways
Biological processes and signaling networks where the TINF2 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
- DYSKERATOSIS CONGENITA AUTOSOMAL DOMINANT 1
- DYSKERATOSIS CONGENITA AUTOSOMAL DOMINANT 3
- Revesz syndrome
- EXUDATIVE RETINOPATHY WITH BONE MARROW FAILURE