decreased skeletal muscle glycogen level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description less than the normal concentration of a readily converted carbohydrate reserve in skeletal muscle (Mammalian Phenotype Ontology, MP_0010399)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010399
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Genes

5 gene mutations causing the decreased skeletal muscle glycogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
GBE1 glucan (1,4-alpha-), branching enzyme 1
GYS1 glycogen synthase 1 (muscle)
PRKAB2 protein kinase, AMP-activated, beta 2 non-catalytic subunit
SAMD4A sterile alpha motif domain containing 4A