Descriptor English: | Glycogen Phosphorylase, Liver Form | ||||||
Descriptor Spanish: |
Glucógeno Fosforilasa de Forma Hepática
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Descriptor Portuguese: | Glicogênio Fosforilase Hepática | ||||||
Descriptor French: | Glycogen phosphorylase, liver form | ||||||
Entry term(s): |
Glycogen Phosphorylase a, Liver Form Glycogen Phosphorylase b, Liver Form |
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Tree number(s): |
D08.811.913.400.450.460.400.186.124 |
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RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D025001 | ||||||
Scope note: | 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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Allowable Qualifiers: |
AD administration & dosage AE adverse effects AI antagonists & inhibitors AN analysis BI biosynthesis BL blood CF cerebrospinal fluid CH chemistry CL classification CS chemical synthesis DE drug effects DF deficiency EC economics GE genetics HI history IM immunology IP isolation & purification ME metabolism PD pharmacology PH physiology PK pharmacokinetics PO poisoning RE radiation effects SD supply & distribution ST standards TO toxicity TU therapeutic use UL ultrastructure UR urine |
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Registry Number: | EC 2.4.1.- | ||||||
Previous Indexing: |
Glucosyltransferases (1966-1971) Phosphorylases (1972-2001) |
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Public MeSH Note: | 2002 |
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History Note: | 2002 |
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Related: |
Glycogen Storage Disease Type VI
MeSH | ||||||
DeCS ID: | 36106 | ||||||
Unique ID: | D025001 | ||||||
Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
Date Established: | 2002/01/01 | ||||||
Date of Entry: | 2001/07/25 | ||||||
Revision Date: | 2003/07/09 |
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CHEMICALS AND DRUGS
Enzymes and Coenzymes [D08]Enzymes and Coenzymes
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Glycogen Phosphorylase, Liver Form
- Preferred
Glycogen Phosphorylase b, Liver Form
- Narrower
Glycogen Phosphorylase a, Liver Form
- Narrower
Concept UI |
M0372890 |
Scope note | 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. |
Preferred term | Glycogen Phosphorylase, Liver Form |
Concept UI |
M0378536 |
Preferred term | Glycogen Phosphorylase b, Liver Form |
Concept UI |
M0378535 |
Preferred term | Glycogen Phosphorylase a, Liver Form |
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