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Symbol
Name
ID
Fktn
fukutin
MGI:2179507
Phenotype annotations related to homeostasis/metabolism
Darker colors indicate more annotations
Human Phenotypes
Elevated circulating creatine kinase concentration
Carnosinuria
Myoglobinuria
Disease(s) Associated with FKTN
autosomal recessive limb-girdle muscular dystrophy type 2L
autosomal recessive limb-girdle muscular dystrophy type 2M
dilated cardiomyopathy 1X
Fukuyama congenital muscular dystrophy
muscular dystrophy
muscular dystrophy-dystroglycanopathy type B4

Mouse Phenotypes
increased circulating creatine kinase level
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)
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
05/14/2024
MGI 6.23
The Jackson Laboratory