abnormal skeletal muscle satellite cell proliferation Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description anomaly in the ability of unfused cells in skeltal muscle to undergo expansion by cell division, usually triggered by injury or disease (Mammalian Phenotype Ontology, MP_0009410)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009410
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6 gene mutations causing the abnormal skeletal muscle satellite cell proliferation phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DMD dystrophin
FOXJ3 forkhead box J3
IL6 interleukin 6
MYF5 myogenic factor 5
PAX7 paired box 7
POMGNT1 protein O-linked mannose N-acetylglucosaminyltransferase 1 (beta 1,2-)