type 1 muscle fiber predominance Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal predominance of type I muscle fibers (in general, this feature can only be observed on muscle biopsy). (Human Phenotype Ontology, HP_0003803)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0003803
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Genes

9 genes associated with the type 1 muscle fiber predominance phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
COL6A1 collagen, type VI, alpha 1
COL6A2 collagen, type VI, alpha 2
COL6A3 collagen, type VI, alpha 3
MYH7 myosin, heavy chain 7, cardiac muscle, beta
NEB nebulin
RYR1 ryanodine receptor 1 (skeletal)
TNNT1 troponin T type 1 (skeletal, slow)
TPM2 tropomyosin 2 (beta)