skeletal muscle 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 tissue; usually due to irreversible damage (Mammalian Phenotype Ontology, MP_0003852)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003852
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Genes

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

Symbol Name
CAV3 caveolin 3
CCL13 chemokine (C-C motif) ligand 13
COL6A1 collagen, type VI, alpha 1
CRYAB crystallin, alpha B
DES desmin
DMD dystrophin
DYSF dysferlin
EGLN2 egl-9 family hypoxia-inducible factor 2
FKRP fukutin related protein
FOXJ3 forkhead box J3
ITGA7 integrin, alpha 7
KY kyphoscoliosis peptidase
LAMA2 laminin, alpha 2
LARGE like-glycosyltransferase
MAML1 mastermind-like 1 (Drosophila)
PAX7 paired box 7
PFKM phosphofructokinase, muscle
PLEC plectin
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SCYL1 SCY1-like 1 (S. cerevisiae)
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SLC8A3 solute carrier family 8 (sodium/calcium exchanger), member 3
TTN titin
VCP valosin containing protein