abnormal gastrocnemius weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly of the weight of the two-headed large muscle of the posterior portion of the lower hindleg, the most superficial of the calf muscles (Mammalian Phenotype Ontology, MP_0013188)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0013188
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10 gene mutations causing the abnormal gastrocnemius weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
FST follistatin
INHBA inhibin, beta A
MSTN myostatin
MTM1 myotubularin 1
MYOZ1 myozenin 1
PLIN1 perilipin 1
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
SEPN1 selenoprotein N, 1
SGCB sarcoglycan, beta (43kDa dystrophin-associated glycoprotein)
SLC4A4 solute carrier family 4 (sodium bicarbonate cotransporter), member 4