|
Symbol Name ID |
Fktn
fukutin MGI:2179507 |
| * | Aspects of the system are reported to show a normal phenotype. |
| Darker colors indicate more annotations |
| Human Phenotypes | Weak cry |
Myalgia |
Exercise-induced myalgia |
| Disease(s) Associated with FKTN | |||
| autosomal recessive limb-girdle muscular dystrophy type 2L | |||
| Fukuyama congenital muscular dystrophy |
| Mouse Phenotypes | behavior/neurological phenotype |
decreased grip strength |
weakness |
|
| Availability | Mouse Genotype | |||
| Fktntm1Kcam/Fktntm1Kcam Tg(CAG-cre/Esr1*)5Amc/? (conditional) |
* | |||
| Fktntm1Kcam/Fktntm1Kcam Tg(Ckmm-cre)5Khn/? (conditional) |
||||
| Fktntm1Kcam/Fktntm1Kcam Myf5tm3(cre)Sor/Myf5+ (conditional) |
||||
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 05/14/2024 MGI 6.23 |
|
|
|
||
Analysis Tools