abnormal skeletal muscle fiber type ratio Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description deviation from the standard ratios of fiber types in a given skeletal muscle compared to control samples (Mammalian Phenotype Ontology, MP_0009409)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0009409
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Genes

26 gene mutations causing the abnormal skeletal muscle fiber type ratio phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
AGRN agrin
ALS2 amyotrophic lateral sclerosis 2 (juvenile)
BCL2 B-cell CLL/lymphoma 2
CFL2 cofilin 2 (muscle)
CISD2 CDGSH iron sulfur domain 2
FOXJ3 forkhead box J3
HBA1 hemoglobin, alpha 1
HSPG2 heparan sulfate proteoglycan 2
ITGA7 integrin, alpha 7
LEP leptin
MB myoglobin
MYH1 myosin, heavy chain 1, skeletal muscle, adult
MYH4 myosin, heavy chain 4, skeletal muscle
MYOZ1 myozenin 1
MYOZ2 myozenin 2
NR1D1 nuclear receptor subfamily 1, group D, member 1
PPP3CA protein phosphatase 3, catalytic subunit, alpha isozyme
PPP3CB protein phosphatase 3, catalytic subunit, beta isozyme
SCYL1 SCY1-like 1 (S. cerevisiae)
SEPN1 selenoprotein N, 1
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4
SMTNL1 smoothelin-like 1
SSPN sarcospan
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