decreased liver 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 liver (Mammalian Phenotype Ontology, MP_0010398)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0010398
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Genes

16 gene mutations causing the decreased liver glycogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACTA1 actin, alpha 1, skeletal muscle
BCS1L BC1 (ubiquinol-cytochrome c reductase) synthesis-like
CAV1 caveolin 1, caveolae protein, 22kDa
EPM2AIP1 EPM2A (laforin) interacting protein 1
FABP3 fatty acid binding protein 3, muscle and heart
GBE1 glucan (1,4-alpha-), branching enzyme 1
GYS2 glycogen synthase 2 (liver)
IL6ST interleukin 6 signal transducer
KLF15 Kruppel-like factor 15
MARK3 MAP/microtubule affinity-regulating kinase 3
MIR122 microRNA 122
NCOR1 nuclear receptor corepressor 1
OPA3 optic atrophy 3 (autosomal recessive, with chorea and spastic paraplegia)
OSMR oncostatin M receptor
PLAU plasminogen activator, urokinase
PRKAB2 protein kinase, AMP-activated, beta 2 non-catalytic subunit