G2Cdb::Allele report
- Mutation type
- MI
Altered genes (1)
Gene |
Symbol |
Species |
Description |
G00001806 |
PLP1 |
Homo sapiens |
proteolipid protein 1 |
Diseases (1)
Disease |
Description |
Nervous effect |
D00000213 |
Spastic paraplegia type 2 (late onset) |
Y |
Literature (1)
Pubmed - other