Descriptor English: | Fragile X Mental Retardation Protein | ||||
Descriptor Spanish: |
Proteína del Retraso Mental del Síndrome del Cromosoma X Frágil
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Descriptor Portuguese: | Proteína do X Frágil de Retardo Mental | ||||
Descriptor French: | Protéine du syndrome X fragile | ||||
Entry term(s): |
FMRP Protein Fragile X Mental Retardation 1 Protein Fragile X Mental Retardation-1 Protein |
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Tree number(s): |
D12.776.157.725.061 D12.776.631.299 D12.776.664.962.124 |
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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. |
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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 |
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Entry Combination: |
deficiency:Fragile X Syndrome
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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 |
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History Note: | 2006(1991) |
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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 |
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CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins -
CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins -
CHEMICALS AND DRUGS
Amino Acids, Peptides, and Proteins [D12]Amino Acids, Peptides, and Proteins
|
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. |
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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