Structured Summary
Abstract
A protein that is highly expressed in the nervous system as well as other tissues; its size and structure vary due to polymorphisms. Expanded CAG TRINUCLEOTIDE REPEATS have been identified in the Huntingtin (HD) Gene of patients with HUNTINGTON DISEASE and are associated with abnormal PROTEIN AGGREGATES. Huntingtin interacts with proteins involved in a variety of gene expression and cellular processes; it is also essential for embryonic development.
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Classification
Broader headings
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Synonyms
2 entry terms
- Huntington Disease Protein
- IT15 Protein
MeSH Record
Aspects Covered
30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, 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
2017
MeSH Record
Previous Indexing
- Nerve Tissue Proteins (2012-2016)
- Nuclear Proteins (1994-2016)
MeSH Hierarchy
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AMA Style
References
- National Library of Medicine. Huntingtin Protein. Medical Subject Headings (MeSH). 2026. Unique ID D000071058. http://id.nlm.nih.gov/mesh/2026/D000071058
- Huntingtin Protein. In: Wikidata. https://www.wikidata.org/wiki/Q24779247