increased glycogen level Gene Set

Dataset MPO Gene-Phenotype Associations
Category disease or phenotype associations
Type phenotype
Description greater than the normal concentration of this readily converted carbohydrate reserve, found in most tissues of the body, especially liver and muscle (Mammalian Phenotype Ontology, MP_0005440)
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39 gene mutations causing the increased glycogen level phenotype in transgenic mice from the MPO Gene-Phenotype Associations dataset.

Symbol Name
ACACB acetyl-CoA carboxylase beta
ADRA1B adrenoceptor alpha 1B
AFP alpha-fetoprotein
ATXN2 ataxin 2
CALR calreticulin
CAV1 caveolin 1, caveolae protein, 22kDa
CKM creatine kinase, muscle
CREBBP CREB binding protein
CTHRC1 collagen triple helix repeat containing 1
CXADR coxsackie virus and adenovirus receptor
DNAJC15 DnaJ (Hsp40) homolog, subfamily C, member 15
EIF2AK3 eukaryotic translation initiation factor 2-alpha kinase 3
EPM2A epilepsy, progressive myoclonus type 2A, Lafora disease (laforin)
FGF21 fibroblast growth factor 21
FNIP1 folliculin interacting protein 1
FSTL1 follistatin-like 1
G6PC glucose-6-phosphatase, catalytic subunit
GAA glucosidase, alpha; acid
GBE1 glucan (1,4-alpha-), branching enzyme 1
GJB1 gap junction protein, beta 1, 32kDa
GNMT glycine N-methyltransferase
GRB10 growth factor receptor-bound protein 10
GSK3A glycogen synthase kinase 3 alpha
H6PD hexose-6-phosphate dehydrogenase (glucose 1-dehydrogenase)
HSD11B1 hydroxysteroid (11-beta) dehydrogenase 1
LEPR leptin receptor
LIFR leukemia inhibitory factor receptor alpha
LPIN1 lipin 1
MAN2C1 mannosidase, alpha, class 2C, member 1
MLXIPL MLX interacting protein-like
NCOA3 nuclear receptor coactivator 3
NHLRC1 NHL repeat containing E3 ubiquitin protein ligase 1
PFKM phosphofructokinase, muscle
PHKA1 phosphorylase kinase, alpha 1 (muscle)
PNPLA2 patatin-like phospholipase domain containing 2
SCG5 secretogranin V
SLC37A4 solute carrier family 37 (glucose-6-phosphate transporter), member 4
STK40 serine/threonine kinase 40
TUB tubby bipartite transcription factor