Fragile X messenger ribonucleoprotein 1

Preferred Label : Fragile X messenger ribonucleoprotein 1;

Symbol : FMR1;

CISMeF acronym : FMR1;

Type : Gene;

Alternative titles and symbols : Fragile X mental retardation protein; FMRP; Fmrp translational regulator 1;

Included titles and symbols : Fragile site, folic acid type, rare, fraxq27.3; FRAXA;

Ensembl ID : ENSG00000102081;

Prefixed ID : *309550;

Details

Origin ID

309550;

UMLS CUI

C1414649;

Automatic exact mappings (from CISMeF team)
- FMR1 Gene [NCIt concept]
- FMR1 gene [LOINC component]
- FMR1 wt Allele [NCIt concept]
- FMRP [LOINC component]
- FRAXA (disorder) [SNOMED CT concept]
- Fragile X Mental Retardation Protein 1 [NCIt concept]
- fragile X mental retardation protein [MeSH concept]
- fragile X messenger ribonucleoprotein 1 [ORDO Gene]
- fragile X messenger ribonucleoprotein 1 [HGNC gene]
- fragile x mental retardation protein [MeSH Descriptor]
- fragile x syndrome [MedlinePlus Topic]
HGNC gene
- fragile X messenger ribonucleoprotein 1 [HGNC gene]
NCIt concept(s)
- FMR1 Gene [NCIt concept]
- FMR1 wt Allele [NCIt concept]
- Fragile X Mental Retardation Protein 1 [NCIt concept]
ORDO concept(s)
- fragile X messenger ribonucleoprotein 1 [ORDO Gene]
Phenotypes related
- Fragile X syndrome [OMIM Phenotype]
- Fragile X tremor/ataxia syndrome [OMIM Phenotype]
- Premature ovarian failure 1 [OMIM Phenotype]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
UMLS correspondences (same concept)
- FMR1 Gene [NCIt concept]
- FMR1 gene [LOINC component]
- fragile X messenger ribonucleoprotein 1 [HGNC gene]

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