ConductScience.org, home

Library / Genes

FMR1: fragile X messenger ribonucleoprotein 1

1 protein, 39 patents, 0 drugs, 0 trials, 4,898 NIH grants and 10,179 papers.

Gene 7

Its symbol and name are HGNC's, unless HGNC and NCBI Gene contradict each other.

FieldValueSource
SymbolFMR1HGNC
Namefragile X messenger ribonucleoprotein 1HGNC
NCBI Gene ID2332NCBI Gene
HGNC IDHGNC:3775HGNC
EnsemblENSG00000102081NCBI Gene
AliasesFMRP, FRAXA, MGC87458, POF, POF1NCBI Gene
Typeprotein-codingNCBI Gene

Proteins 1

Reviewed human proteins whose Swiss-Prot entry states the gene.

UniProt entryProteinLengthStructuresGene stated inSource
Q06787Fragile X messenger ribonucleoprotein 163212Ensembl, GeneID, HGNCUniProt

Patents 39

Patents whose sequence listing holds the protein exactly: the same sequence, by SHA-256, length and CRC-64. A sequence a patent lists is not always one it claims.

PublicationPublishedSEQ ID NOProteinSource
JP 2026004568 A2026-01-1446671Q06787Espacenet
EP 4650780 A22025-11-198781Q06787Espacenet
EP 4641201 A22025-10-298989Q06787Espacenet
JP 2025111747 A2025-07-30136Q06787Espacenet
JP 2025517969 A2025-06-128989Q06787Espacenet
JP 2025517970 A2025-06-128781Q06787Espacenet
WO 2024261220 A12024-12-2613Q06787Espacenet
JP 2024112982 A2024-08-214348Q06787Espacenet
US 11946082 B22024-04-027Q06787Espacenet
JP 2023549761 A2023-11-29229Q06787Espacenet

Drugs 0

Drugs a ChEMBL mechanism record says act on the gene's protein, through Open Targets.

DrugChEMBL IDMechanismActionSource

Trials 0

Trials of those drugs. A trial joins the gene only through a drug that acts on it.

TrialDrugPhaseResults first postedSource

NIH grants 4898

NIH projects whose papers are about the gene, through NIH's grant-paper links.

ProjectTitleIts papers about the geneNewest fiscal yearSource
R01HD036071Genotype-Phenotype Relationships in Fragile X Families2922,025NIH's project files
P50HD103526MIND Institute Intellectual and Developmental Disabilities Research Center592,025NIH's project files
ZIADK057808Understanding the mutational mechanism responsible for the Repeat Expansion Diseases342,025NIH's project files
ZIADK057602The consequences of the unusual mutation responsible for the Repeat Expansion Diseases322,025NIH's project files
R01MH107573Emergence, stability, and predictors of anxiety in Fragile X syndrome272,025NIH's project files
UL1TR001860UC Davis Clinical and Translational Science Center272,025NIH's project files
T32MH019908Research Training for Child Psychiatry and Neurodevelopment252,025NIH's project files
T32HD007489Post-Doctoral Training in Intellectual and Developmental Disabilities Research202,025NIH's project files
R01HD082110Adults with Fragile X Syndrome: Health and Life Course Trajectories172,025NIH's project files
R01MH091131A Family Genetic Study of Autism and Fragile X Syndrome172,025NIH's project files

Papers 10179

Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.

PMIDFound bySource
42825656PubTator, text miningPubMed
42818463PubTator, text miningPubMed
42787895PubTator, text miningPubMed
42787119PubTator, text miningPubMed
42777228PubTator, text miningPubMed
42772924PubTator, text miningPubMed
42772432PubTator, text miningPubMed
42764220PubTator, text miningPubMed
42762881PubTator, text miningPubMed
42724890PubTator, text miningPubMed

The same record as JSON

Release gene-search-2026-11-11-0.1.0

ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

ChEMBL, through Open Targets: CC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence

ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

EMBL-EBI's patent proteins: EMBL-EBI's patent protein files from the EPO, JPO, KIPO and USPTO. EMBL-EBI: "EMBL-EBI itself places no additional restrictions on the use or redistribution of the data available via its Data Resources and Tools other than those provided by the original data owners" and "EMBL-EBI expects attribution (e.g. in publications, services or products) for the use of any of its Data Resources and Tools." Read on 11 Nov 2026 at https://www.ebi.ac.uk/about/terms-of-use

GenBank's patent files: GenBank's patent files. NCBI: "NCBI places no restrictions on the use or distribution of the GenBank data. However, some submitters may claim patent, copyright, or other intellectual property rights in all or a portion of the data they have submitted." Read on 11 Nov 2026 at https://www.ncbi.nlm.nih.gov/genbank/about/

HGNC: CC0: https://www.genenames.org/about/license/

NCBI Gene: None named for the file. NCBI says information created by or for the US government on its site is in the public domain, and asks that NLM be acknowledged: https://www.ncbi.nlm.nih.gov/home/about/policies/

NIH's project files and grant-paper links: Public domain (NIH RePORTER)

Open Targets: CC0 1.0. Open Targets asks that users cite its latest paper: Buniello et al. 2025, Open Targets Platform: facilitating therapeutic hypotheses building in drug discovery, Nucleic Acids Research 53(D1):D1467, PMID 39657122. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence

PubTator 3: Public domain

UniProt: CC BY 4.0. UniProt's licence file: "All databases and documents in the UniProt FTP directory may be copied and redistributed freely, without advance permission, provided that this copyright statement is reproduced with each copy." UniProt asks that users cite its latest paper: The UniProt Consortium, UniProt: the Universal Protein Knowledgebase in 2025, Nucleic Acids Research 53:D609-D617, https://doi.org/10.1093/nar/gkae1010. Read on 9 Nov 2026 at https://www.uniprot.org/help/license