Structured Summary
Abstract
An isoenzyme of GLYCOGEN PHOSPHORYLASE that catalyzes the degradation of GLYCOGEN in liver tissue. Mutation of the gene coding this enzyme on chromosome 14 is the cause of GLYCOGEN STORAGE DISEASE TYPE VI.
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Synonyms
3 entry terms
- Glycogen Phosphorylase, Liver Form
- Glycogen Phosphorylase a, Liver Form
- Glycogen Phosphorylase b, Liver Form
MeSH Record
Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2002
MeSH Record
Previous Indexing
- Glucosyltransferases (1966-1971)
- Phosphorylases (1972-2001)
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References
- National Library of Medicine. Liver Form Glycogen Phosphorylase. Medical Subject Headings (MeSH). 2026. Unique ID D025001. http://id.nlm.nih.gov/mesh/2026/D025001
- Liver Form Glycogen Phosphorylase. In: Wikidata. https://www.wikidata.org/wiki/Q21121196