decreased skeletal muscle weight Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than average skeletal muscle weight (Mammalian Phenotype Ontology, MP_0010239)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010239
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Genes

14 gene mutations causing the decreased skeletal muscle weight phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
BARX2 BARX homeobox 2
COL12A1 collagen, type XII, alpha 1
COL6A3 collagen, type VI, alpha 3
EFEMP1 EGF containing fibulin-like extracellular matrix protein 1
FST follistatin
HOXC10 homeobox C10
MTOR mechanistic target of rapamycin (serine/threonine kinase)
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
SLC6A6 solute carrier family 6 (neurotransmitter transporter), member 6
WFIKKN1 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 1
WFIKKN2 WAP, follistatin/kazal, immunoglobulin, kunitz and netrin domain containing 2
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