absent skeletal muscle Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description absence of any of the striated muscle fibers connected at either or both extremities with the bony framework of the body (Mammalian Phenotype Ontology, MP_0004846)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004846
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4 gene mutations causing the absent skeletal muscle phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CACNA1S calcium channel, voltage-dependent, L type, alpha 1S subunit
MET MET proto-oncogene, receptor tyrosine kinase
MYLPF myosin light chain, phosphorylatable, fast skeletal muscle
PAX3 paired box 3