|
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 | Intrauterine growth retardation |
| Disease(s) Associated with FKTN | |
| Fukuyama congenital muscular dystrophy |
| Mouse Phenotypes | decreased embryo size |
growth/size/body region phenotype |
decreased body weight |
postnatal growth retardation |
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| Availability | Mouse Genotype | ||||
| Fktntm1Ttd/Fktntm1Ttd | |||||
| Fktntm1Kcam/Fktntm1Kcam Tg(CAG-cre/Esr1*)5Amc/? (conditional) |
* | ||||
| Fktntm1Kcam/Fktntm1Kcam Myf5tm3(cre)Sor/Myf5+ (conditional) |
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| Fktntm3.1Ttd/Fktntm3.1Ttd Myf5tm3(cre)Sor/Myf5+ (conditional) |
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO) |
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last database update 05/14/2024 MGI 6.23 |
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