muscle fiber inclusion bodies Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0100299
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Genes

11 genes associated with the muscle fiber 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
MYH2 myosin, heavy chain 2, skeletal muscle, adult
MYOT myotilin
NEB nebulin
RYR1 ryanodine receptor 1 (skeletal)
TNNT1 troponin T type 1 (skeletal, slow)
TPM2 tropomyosin 2 (beta)
TPM3 tropomyosin 3