dystrophic muscle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0000752
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Genes

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

Symbol Name
CAPN3 calpain 3, (p94)
CAV3 caveolin 3
CHKB choline kinase beta
DAG1 dystroglycan 1 (dystrophin-associated glycoprotein 1)
DMD dystrophin
DTNA dystrobrevin, alpha
DYSF dysferlin
FKRP fukutin related protein
HTRA2 HtrA serine peptidase 2
ITGA7 integrin, alpha 7
LAMA2 laminin, alpha 2
LARGE like-glycosyltransferase
LMNA lamin A/C
MAML1 mastermind-like 1 (Drosophila)
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)
SCN8A sodium channel, voltage gated, type VIII alpha subunit
SCYL1 SCY1-like 1 (S. cerevisiae)
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SGCD sarcoglycan, delta (35kDa dystrophin-associated glycoprotein)
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
SYNE1 spectrin repeat containing, nuclear envelope 1
TLN2 talin 2
TRIM32 tripartite motif containing 32
TTN titin
ZMPSTE24 zinc metallopeptidase STE24