Structured Summary
Abstract
A RNA-binding protein that is found predominately in the CYTOPLASM. It helps regulate GENETIC TRANSLATION in NEURONS and is absent or under-expressed in FRAGILE X SYNDROME.
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Classification
Broader headings
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MeSH Record
Synonyms
5 entry terms
- FMR1 Protein
- FMRP Protein
- Fragile X Mental Retardation Protein
- Fragile X Mental Retardation-1 Protein
- Fragile X Mental Retardation 1 Protein
MeSH Record
Aspects Covered
29 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, 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
2006(1991)
MeSH Hierarchy
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AMA Style
References
- National Library of Medicine. Fragile X Messenger Ribonucleoprotein 1. Medical Subject Headings (MeSH). 2026. Unique ID D051860. http://id.nlm.nih.gov/mesh/2026/D051860
- Fragile X Messenger Ribonucleoprotein 1. In: Wikidata. https://www.wikidata.org/wiki/Q58622761