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Breast, colorectal, testis, urothelial, renal, hepatocellular and gynaecological cancers showed moderate to strong cytoplasmic positivity. Remaining cancer tissues were generally negative.
Most hepatocellular carcinomas as well as a majority of renal, urothelial and testicular cancers along with several cases of melanoma showed moderate to strong cytoplasmic immunoreactivity. Remaining cancer tissues were weakly stained or negative.
GENE INFORMATION
Gene name
PYGL
Synonyms
Description
Phosphorylase, glycogen, liver (HGNC Symbol)
Entrez gene summary
This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively. The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues. In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly. Alternative splicing results in multiple transcript variants encoding different isoforms.[provided by RefSeq, Feb 2011]
P06737 [Direct mapping] Glycogen phosphorylase, liver form
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Enzymes ENZYME proteins Transferases SPOCTOPUS predicted membrane proteins Predicted intracellular proteins Plasma proteins Disease related genes Potential drug targets Protein evidence (Kim et al 2014) Protein evidence (Ezkurdia et al 2014)
P06737 [Direct mapping] Glycogen phosphorylase, liver form
Show all
Enzymes ENZYME proteins Transferases SPOCTOPUS predicted membrane proteins Predicted intracellular proteins Plasma proteins Disease related genes Potential drug targets Protein evidence (Kim et al 2014) Protein evidence (Ezkurdia et al 2014)