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Human Disease and Mouse Model Detail
Human Disease Myopathy, Congenital, with Fiber-Type Disproportion; CFTD
OMIM ID: 255310
Synonyms Fiber-Type Disproportion Myopathy, Congenital; CFTDM; Myopathy, Congenital
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Mouse Homologs Human Homologs Mouse Models Mouse : Human
Homology Class
     Acta1 ACTA1*   1:1 Homology
Myh7 MYH7*   1:1 Homology
Ryr1 RYR1*   1:1 Homology
Sepn1 SEPN1*   1:1 Homology
TPM2*   0:1 Homology
Tpm3 TPM3*   1:1 Homology

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 5.21
The Jackson Laboratory