abnormal muscle weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description any anomaly in the average muscle weight (Mammalian Phenotype Ontology, MP_0004233)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0004233
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30 gene mutations causing the abnormal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
ARNTL aryl hydrocarbon receptor nuclear translocator-like
BARX2 BARX homeobox 2
BCKDK branched chain ketoacid dehydrogenase kinase
CCL13 chemokine (C-C motif) ligand 13
CHRNE cholinergic receptor, nicotinic, epsilon (muscle)
COL12A1 collagen, type XII, alpha 1
COL6A3 collagen, type VI, alpha 3
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
FST follistatin
GARS glycyl-tRNA synthetase
GRB10 growth factor receptor-bound protein 10
HOXC10 homeobox C10
INHBA inhibin, beta A
INHBB inhibin, beta B
LEPR leptin receptor
MSTN myostatin
MTM1 myotubularin 1
MTOR mechanistic target of rapamycin (serine/threonine kinase)
NMNAT2 nicotinamide nucleotide adenylyltransferase 2
NOS1 nitric oxide synthase 1 (neuronal)
PAX7 paired box 7
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
RPS6KB1 ribosomal protein S6 kinase, 70kDa, polypeptide 1
SGCA sarcoglycan, alpha (50kDa dystrophin-associated glycoprotein)
SLC6A6 solute carrier family 6 (neurotransmitter transporter), member 6
TLL2 tolloid-like 2
TRIM32 tripartite motif containing 32
WFIKKN1 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
WFIKKN2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2