skeletal muscle hypertrophy Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description Hypertrophy (increase in size) of muscle cells (as opposed to hyperplasia, which refers to an increase in the number of muscle cells). (Human Phenotype Ontology, HP_0003712)
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7 gene mutations causing the skeletal muscle hypertrophy phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
DMD dystrophin
MSTN myostatin
SEPN1 selenoprotein N, 1
SGCG sarcoglycan, gamma (35kDa dystrophin-associated glycoprotein)
TCF15 transcription factor 15 (basic helix-loop-helix)
TRDN triadin
TRIM55 tripartite motif containing 55