abnormal sarcolemma morphology Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any structural anomaly in the plasma membrane of a muscle fiber that is capable of conducting electrical impulses (Mammalian Phenotype Ontology, MP_0004121)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004121
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11 gene mutations causing the abnormal sarcolemma morphology phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CAPN3 calpain 3, (p94)
CAV3 caveolin 3
CHKB choline kinase beta
COL12A1 collagen, type XII, alpha 1
COL13A1 collagen, type XIII, alpha 1
DMD dystrophin
DYSF dysferlin
LAMA2 laminin, alpha 2
PTCD2 pentatricopeptide repeat domain 2
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)