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