fragile X messenger ribonucleoprotein 1

Summary
Gene Symbol
  • FMR1
Organism
Homo sapiens (human)
NCBI Gene
2332
PubChem
2332
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Acetylation
  • Activator
  • Alternative splicing
  • Cell membrane
  • Cell projection
  • Centromere
  • Chromosome
  • Cytoplasm
  • DNA damage
  • Disease variant
  • Host-virus interaction
  • Intellectual disability
  • Methylation
  • Neurodegeneration
  • Neurogenesis
  • Nucleus
  • Phosphoprotein
  • Postsynaptic cell membrane
  • Premature ovarian failure
  • RNA-binding
  • RNA-mediated gene silencing
  • Reference proteome
  • Repeat
  • Repressor
  • Ribonucleoprotein
  • Synaptosome
  • Translation regulation
  • Ubl conjugation
  • mRNA splicing
  • mRNA transport
Proteins
Displaying 1 entry
UniProt Protein Name
Q06787
  • Fragile X messenger ribonucleoprotein
  • Protein FMR-1
Gene Ontology (GO)
GO Hierarchy
Displaying entries 41 - 44 of 44 in total
GO Term Evidence Code PMID
postsynapse
dendritic filopodium
growth cone filopodium
ribonucleoprotein complex
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying all 3 entries
DO ID Disease Name Source
DOID:0050879 fragile X-associated tremor/ataxia syndrome
DOID:0080857 primary ovarian insufficiency 1
DOID:14261 fragile X syndrome

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 4, 2025