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Symbol
Name
ID
Fktn
fukutin
MGI:2179507
Phenotype annotations related to homeostasis/metabolism
*Aspects of the system are reported to show a normal phenotype.
Darker colors indicate more annotations
Human Phenotypes
Elevated serum creatine kinase
Abnormal glycosylation
Disease(s) Associated with FKTN
autosomal recessive limb-girdle muscular dystrophy type 2M
congenital muscular dystrophy-dystroglycanopathy type A1
Fukuyama congenital muscular dystrophy
muscular dystrophy-dystroglycanopathy

Mouse Phenotypes
homeostasis/metabolism phenotype
increased circulating creatine kinase level
Availability Mouse Genotype
Fktntm3(FKTN)Ttd/Fktntm3(FKTN)Ttd *
Fktntm1Kcam/Fktntm1Kcam
Tg(CAG-cre/Esr1*)5Amc/?  (conditional)
Fktntm1Kcam/Fktntm1Kcam
Tg(Ckmm-cre)5Khn/?  (conditional)
Fktntm1Kcam/Fktntm1Kcam
Myf5tm3(cre)Sor/Myf5+  (conditional)
Fktntm3.1Ttd/Fktntm3.1Ttd
Myf5tm3(cre)Sor/Myf5+  (conditional)
Fktntm3.1Ttd/Fktntm3.1Ttd
Tg(Ckmm-cre)5Khn/0  (conditional)

Contributing Projects:
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
11/12/2019
MGI 6.14
The Jackson Laboratory