Symbol Name ID |
Rtn2
reticulon 2 (Z-band associated protein) MGI:107612 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Lower limb muscle weakness |
Lower limb spasticity |
Spastic paraplegia |
Progressive spastic paraplegia |
Spastic gait |
Difficulty walking |
Muscle spasm |
Lower limb amyotrophy |
Disease(s) Associated with RTN2 | ||||||||
hereditary spastic paraplegia 12 |
Mouse Phenotypes | muscle phenotype |
decreased muscle cell glucose uptake |
|
Availability | Mouse Genotype | ||
Rtn2tm1Lex/Rtn2tm1Lex | * | ||
Rtn2tm1Lex/Rtn2+ |
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
||
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support. |
last database update 05/28/2024 MGI 6.13 |
|
|