Details
| Type | Protein Coding |
| Official Symbol | NDN |
| Official Name | necdin, MAGE family member [Source:HGNC Symbol;Acc:HGNC:7675] |
| Ensembl ID | ENSG00000288364 |
| Bio databases IDs | |
| Aliases | necdin, MAGE family member |
| 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