G2Cdb::Allele report
- Mutation type
- SNP
Altered genes (1)
Gene |
Symbol |
Species |
Description |
G00000027 |
GRIN2B |
Homo sapiens |
glutamate receptor, ionotropic, N-methyl D-aspartate 2B |
Diseases (1)
Disease |
Description |
Nervous effect |
D00000166 |
Schizophrenia |
Y |
Literature (1)
Pubmed - human_disease