skeletal muscle fiber degeneration Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description pathological deterioration of skeletal muscle fiber tissue, often accompanied by loss of function (Mammalian Phenotype Ontology, MP_0009412)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009412
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Genes

11 gene mutations causing the skeletal muscle fiber degeneration phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BAG3 BCL2-associated athanogene 3
CFL2 cofilin 2 (muscle)
DMD dystrophin
DYSF dysferlin
EPG5 ectopic P-granules autophagy protein 5 homolog (C. elegans)
FKRP fukutin related protein
LARGE like-glycosyltransferase
MYH4 myosin, heavy chain 4, skeletal muscle
MYOF myoferlin
PFKM phosphofructokinase, muscle
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)