Details
| Type | Protein Coding |
| Official Symbol | SLC25A24 |
| Official Name | solute carrier family 25 member 24 [Source:HGNC Symbol;Acc:HGNC:20662] |
| Ensembl ID | ENSG00000284468 |
| Bio databases IDs | |
| Aliases | solute carrier family 25 member 24 |
| 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
- FONTAINE PROGEROID SYNDROME
- Gorlin-Chaudhry-Moss syndrome (GCMS); Syndrome with Hypertrichosis Progeroid Appearance and Mitochondrial Dysfunction