G2Cdb::Human Disease report
- Disease id
- D00000170
- Name
- Bipolar disorder
- Nervous system disease
- yes
Genes (8)
| Gene | Name/Description | Mutations Found | Literature | Mutations Type | Genetic association? |
|---|---|---|---|---|---|
| G00001807 | MBP myelin basic protein |
Y | (8723042) | Translocation (T) | N |
| G00002098 | GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1 |
Y | (12610658) | Single nucleotide polymorphism (SNP) | Y |
| G00002098 | GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1 |
Y | (16969270) | Single nucleotide polymorphism (SNP) | N |
| G00002098 | GRIN1 glutamate receptor, ionotropic, N-methyl D-aspartate 1 |
Y | (16969270) | Microsatellite polymorphism (MSP) | N |
| G00001821 | SHANK2 SH3 and multiple ankyrin repeat domains 2 |
N | (15118355) | Repeat polymorphism (RP) | N |
| G00001821 | SHANK2 SH3 and multiple ankyrin repeat domains 2 |
N | (12895207) | Repeat polymorphism (RP) | N |
| G00002208 | AKAP5 A kinase (PRKA) anchor protein 5 |
Y | (16434481) | Copy Number Polymorphism (CNP) | Y |
| G00001420 | GSK3B glycogen synthase kinase 3 beta |
Y | (16289783) | Polymorphism (P) | N |
| G00001420 | GSK3B glycogen synthase kinase 3 beta |
Y | (16528748) | Single nucleotide polymorphism (SNP) | N |
| G00001420 | GSK3B glycogen synthase kinase 3 beta |
Y | (17357145) | Copy Number Polymorphism (CNP) | Y |
| G00000030 | NOS1 nitric oxide synthase 1 (neuronal) |
Y | (14681919) | Single nucleotide polymorphism (SNP) | N |
| G00000027 | GRIN2B glutamate receptor, ionotropic, N-methyl D-aspartate 2B |
Y | (16549338) | Polymorphism (P) | Y |
| G00001324 | ATP1A1 ATPase, Na+/K+ transporting, alpha 1 polypeptide |
Y | (9646882) | Dinucleotide polymorphism (DNP) | Y |