muscle fiber cytoplasmatic inclusion bodies Gene Set

Dataset	HPO Gene-Disease Associations
Category	disease or phenotype associations
Type	phenotype
Description	The presence of inclusion bodies within the cytoplasm of muscle cells. Inclusion bodies are aggregates (deposits) or stainable material, usually misfolded proteins. (Human Phenotype Ontology, HP_0100303)
External Link	http://compbio.charite.de/hpoweb/showterm?id=HP:0100303
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Genes

10 genes associated with the muscle fiber cytoplasmatic inclusion bodies phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol	Name
ACTA1	actin, alpha 1, skeletal muscle
CFL2	cofilin 2 (muscle)
FLNC	filamin C, gamma
KBTBD13	kelch repeat and BTB (POZ) domain containing 13
MYOT	myotilin
NEB	nebulin
RYR1	ryanodine receptor 1 (skeletal)
TNNT1	troponin T type 1 (skeletal, slow)
TPM2	tropomyosin 2 (beta)
TPM3	tropomyosin 3