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Descriptor English: Fragile X Mental Retardation Protein
Descriptor Spanish: Proteína de la Discapacidad Intelectual del Síndrome del Cromosoma X Frágil
Descriptor proteína de la discapacidad intelectual del síndrome del cromosoma X frágil
Entry term(s) proteína del retraso mental del síndrome del cromosoma X frágil
Scope note: Proteína que se une al ARN y que se encuentra principalmente en el CITOPLASMA. Ayuda a regular la TRADUCCIÓN GENÉTICA en las NEURONAS y está ausente o infraexpresada en el SÍNDROME DEL CROMOSOMA X FRÁGIL.
Descriptor Portuguese: Proteína do X Frágil da Deficiência Intelectual
Descriptor French: Protéine du syndrome X fragile
Entry term(s): FMRP Protein
Fragile X Mental Retardation 1 Protein
Fragile X Mental Retardation-1 Protein
Tree number(s): D12.776.157.725.061
D12.776.631.299
D12.776.664.962.124
RDF Unique Identifier: https://id.nlm.nih.gov/mesh/D051860
Scope note: 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. In DeCS, some entry terms may include outdated and offensive terms according to The United Nations Convention on the Rights of Persons with Disabilities (UNCRPD) in order to assist users who are interested in retrieving comprehensive search results for studies such as in longitudinal studies.
Allowable Qualifiers: AD administration & dosage
AE adverse effects
AG agonists
AI antagonists & inhibitors
AN analysis
BI biosynthesis
BL blood
CF cerebrospinal fluid
CH chemistry
CL classification
CS chemical synthesis
DE drug effects
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
Entry Combination: deficiency:Fragile X Syndrome
Registry Number: 139135-51-6
Public MeSH Note: 2006; FRAGILE X MENTAL RETARDATION PROTEIN was indexed under NERVE TISSUE PROTEINS & RNA-BINDING PROTEINS 1991-2005
History Note: 2006(1991)
DeCS ID: 50923
Unique ID: D051860
Documents indexed in the Virtual Health Library (VHL): Click here to access the VHL documents
Date Established: 2006/01/01
Date of Entry: 2005/06/30
Revision Date: 2015/11/23
Fragile X Mental Retardation Protein - Preferred
Concept UI M0188653
Scope note 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. In DeCS, some entry terms may include outdated and offensive terms according to The United Nations Convention on the Rights of Persons with Disabilities (UNCRPD) in order to assist users who are interested in retrieving comprehensive search results for studies such as in longitudinal studies.
Preferred term Fragile X Mental Retardation Protein
Entry term(s) FMRP Protein
Fragile X Mental Retardation 1 Protein
Fragile X Mental Retardation-1 Protein



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