muscle fatigue Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description An abnormal, increased fatiguability of the musculature. (Human Phenotype Ontology, HP_0003750)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0003646
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Genes

11 gene mutations causing the muscle fatigue phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ATP2A1 ATPase, Ca++ transporting, cardiac muscle, fast twitch 1
COMP cartilage oligomeric matrix protein
DMD dystrophin
EIF4H eukaryotic translation initiation factor 4H
KCNJ11 potassium channel, inwardly rectifying subfamily J, member 11
MB myoglobin
MTMR14 myotubularin related protein 14
NOS1 nitric oxide synthase 1 (neuronal)
PPARGC1A peroxisome proliferator-activated receptor gamma, coactivator 1 alpha
SCN4A sodium channel, voltage gated, type IV alpha subunit
SLC2A4 solute carrier family 2 (facilitated glucose transporter), member 4