abnormal glycogen catabolism Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description inability to breakdown glycogen; or reduced or increased rate of glycogen breakdown (Mammalian Phenotype Ontology, MP_0002713)
External Link http://www.informatics.jax.org/searches/Phat.cgi?id=MP:0002713
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10 gene mutations causing the abnormal glycogen catabolism phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
CEBPB CCAAT/enhancer binding protein (C/EBP), beta
CKM creatine kinase, muscle
GBE1 glucan (1,4-alpha-), branching enzyme 1
GYS1 glycogen synthase 1 (muscle)
GYS2 glycogen synthase 2 (liver)
HMGB1 high mobility group box 1
MGAM maltase-glucoamylase
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1
PITPNA phosphatidylinositol transfer protein, alpha
PRKAB2 protein kinase, AMP-activated, beta 2 non-catalytic subunit