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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fktn
fukutin
MGI:2179507
11 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Dysfim/Dysf+
Fktntm1Ttd/Fktntm2(FCMD)Ttd
involves: 129S7/SvEvBrd * C57BL/6 * SJL/J
normal muscle phenotype J:221523
Dysfim/Dysfim
Fktntm1Ttd/Fktntm2(FCMD)Ttd
involves: 129S7/SvEvBrd * C57BL/6 * SJL/J
abnormal skeletal muscle fiber morphology J:221523
abnormal skeletal muscle morphology J:221523
centrally nucleated skeletal muscle fibers J:221523
dystrophic muscle J:221523
myositis J:221523
skeletal muscle fiber degeneration J:221523
skeletal muscle fibrosis J:221523
Dysfim/Dysfim
Fktntm2(FCMD)Ttd/Fktn+
involves: C57BL/6 * SJL/J
abnormal skeletal muscle fiber morphology J:221523
centrally nucleated skeletal muscle fibers J:221523
dystrophic muscle J:221523
skeletal muscle fiber necrosis J:221523
Fktntm1Ttd/Fktntm2(FCMD)Ttd
involves: 129S7/SvEvBrd
abnormal enzyme/coenzyme activity J:144746
abnormal neuronal migration J:144746
normal muscle phenotype J:144746
Fktntm2(FCMD)Ttd/Fktntm2(FCMD)Ttd
Not Specified
abnormal enzyme/coenzyme activity J:114512, J:144746
normal muscle phenotype J:144746

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
12/10/2019
MGI 6.14
The Jackson Laboratory