Details
| Type | Protein Coding |
| Official Symbol | MAGEL2 |
| Official Name | MAGE family member L2 [Source:HGNC Symbol;Acc:HGNC:6814] |
| Ensembl ID | ENSG00000288188 |
| Bio databases IDs | |
| Aliases | MAGE family member L2 |
| 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
- PRADER-WILLI SYNDROME
- SCHAAF-YANG SYNDROME