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Human Disease and Mouse Model Detail
Human Disease Myopathy, Congenital, with Fiber-Type Disproportion; CFTD
OMIM ID: 255310
Human Phenotype Ontology associations
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...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     ACTA1* Acta1   HomoloGene and HGNC
MYH7* Myh7   HomoloGene and HGNC
RYR1* Ryr1   HomoloGene and HGNC
SELENON* Selenon   HomoloGene and HGNC
TPM2* Tpm2   HGNC
TPM3* Tpm3   HomoloGene and HGNC

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 6.07
The Jackson Laboratory