skeletal muscle fiber necrosis Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description morphological changes resulting from pathological death of skeletal muscle fiber tissue; usually due to irreversible damage (Mammalian Phenotype Ontology, MP_0009414)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009414
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Genes

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

Symbol Name
CAV3 caveolin 3
CRYAB crystallin, alpha B
DES desmin
DMD dystrophin
DYSF dysferlin
FKRP fukutin related protein
LAMA2 laminin, alpha 2
LARGE like-glycosyltransferase
MAML1 mastermind-like 1 (Drosophila)
PFKM phosphofructokinase, muscle
PLEC plectin
SCYL1 SCY1-like 1 (S. cerevisiae)
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SLC8A3 solute carrier family 8 (sodium/calcium exchanger), member 3
TTN titin
VCP valosin containing protein