increased skeletal muscle mass Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description increase in the physical bulk, or total amount of matter contained within skeletal muscle (Mammalian Phenotype Ontology, MP_0004818)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004818
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Genes

15 gene mutations causing the increased skeletal muscle mass phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CLCN1 chloride channel, voltage-sensitive 1
DMD dystrophin
DNM2 dynamin 2
FBN2 fibrillin 2
HSPG2 heparan sulfate proteoglycan 2
INHBA inhibin, beta A
INHBB inhibin, beta B
INPP5K inositol polyphosphate-5-phosphatase K
MSTN myostatin
PCSK1 proprotein convertase subtilisin/kexin type 1
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