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 |
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