ConductScience.org, home

Gene · 57532

NUFIP2: nuclear FMR1 interacting protein 2

12 sourcesgene-search-2026-11-11-0.2.0

Download JSON
Cite this record

ConductScience Library. NUFIP2: nuclear FMR1 interacting protein 2. Genes, record 57532. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/57532

On this page

Gene

Symbol
NUFIP2
HGNC
Name
nuclear FMR1 interacting protein 2
HGNC
NCBI Gene ID
57532
NCBI Gene
HGNC ID
HGNC:17634
HGNC
Ensembl
ENSG00000108256
NCBI Gene
Aliases
182-FIP, 82-FIP, FIP-82, KIAA1321, MGC117262, NUFP2, PIG1
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
Q7Z417FMR1-interacting protein NUFIP26950Ensembl, GeneID, HGNC

Source UniProt

Patents14

Patents whose sequence listing contains this protein's exact sequence. A patent can list a sequence without claiming it.

PublicationPublishedSEQ ID NOProteinSource
JP 2026004568 A2026-01-1456053Q7Z417Espacenet
EP 4650780 A22025-11-19625Q7Z417Espacenet
EP 4641201 A22025-10-29439Q7Z417Espacenet
JP 2025517969 A2025-06-12439Q7Z417Espacenet
JP 2025517970 A2025-06-12625Q7Z417Espacenet
US 11446398 B22022-09-2058133Q7Z417Espacenet
JP 2022524081 A2022-04-27161104Q7Z417Espacenet
US 11078247 B22021-08-037764Q7Z417Espacenet
JP 2019054813 A2019-04-11236488Q7Z417Espacenet
JP 2017121241 A2017-07-13236488Q7Z417Espacenet

1 to 10 of 14

See all 14 patents

Drugs0

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

None in this release.

Trials0

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

None in this release.

NIH grants1,358

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

GrantTitleNUFIP2 papersNewest fiscal year
P40OD010440Caenorhabditis Genetics Center72025
R01MH101221Rare Mutations and Autism Spectrum Disorders72025
P30CA008748Cancer Center Support Grant52025
R01HD036071Genotype-Phenotype Relationships in Fragile X Families52025
ZIAAG000393Influence of Post-transcriptional Gene Regulation on Cell Senescence and Aging52025
ZIAAG000511Post-transcriptional control of Proliferation, Stress Response & Carcinogenesis52025
P30CA016672Cancer Center Support Grant42025
P30CA046934University of Colorado Cancer Center Support Grant32025
P50HD103525WASHINGTON UNIVERSITY INTELLECTUAL AND DEVELOPMENTAL DISABILITIES RESEARCH CENTER32025
R01MH100175Proteogenetics of Autism Spectrum Disorders32025

1 to 10 of 1,358Source NIH's project files

See all 1,358 nih grants

Papers1,424

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

TitleJournalYearPMIDFound bySource
Substrate Profiling of RNF216 Uncovers a Translation-Linked OTUD4 Regulatory Axis.bioRxiv202642817983PubTator, text miningPubMed
The m⁶A reader YTHDF2 regulates mRNA transport and axon outgrowth in developing neurons.Nat Commun202642669734PubTator, text miningPubMed
Massively parallel characterization of RNA G-quadruplex stability and molecular recognition.Nucleic Acids Res202642635121PubTator, text miningPubMed
The KIF6-RBP Complex Orchestrates mRNA Transport Required for Sperm Flagellar Assembly.Adv Sci (Weinh)202642348434PubTator, text miningPubMed
Downregulation of Lonp1 Promotes Melanocyte Pyroptosis via Suppressing Mitophagy and Activating NLRP3 Pathway in Vitiligo under Oxidative Stress.Inflammation202642310240PubTator, text miningPubMed
Single-cell mapping of regulatory DNA-protein interactions.Cell202642242226PubTator, text miningPubMed
TPX2 as a prognostic biomarker and potential therapeutic target for malignant melanoma proliferation and metastasis.Exp Ther Med202642199350PubTator, text miningPubMed
Epigenetic downregulation of MAPKAPK2 exacerbates oxidative stress-induced damage in vitiligo melanocyte cell line model.Front Med (Lausanne)202642089058PubTator, text miningPubMed
Integrated genetic analysis reveals synaptic m6A enrichment in high-risk autism genes.Front Mol Neurosci202641938159PubTator, text miningPubMed
Correction: A missense variant in the KH0-domain of FMRP downregulates the protein in a patient with the clinical hallmarks of fragile X syndrome.Eur J Hum Genet202641917267PubTator, text miningPubMed

1 to 10 of 1,424

See all 1,424 papers

Sources 12

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ChEMBL, through Open TargetsCC BY-SA 3.0
  • ClinicalTrials.govNo license stated
  • EMBL-EBI's patent proteinsNo added restrictions. Attribution expected
  • GenBank's patent filesNo restrictions from NCBI. Submitters may hold rights
  • HGNCCC0
  • NCBI GenePublic domain (US government)
  • NIH's project files and grant-paper linksPublic domain
  • Open TargetsCC0 1.0
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC BY 4.0
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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
  • ChEMBL, through Open TargetsCC BY-SA 3.0, for the parts from ChEMBL. Read on 8 Nov 2026 at https://platform-docs.opentargets.org/licence
  • ClinicalTrials.govnone stated
  • EMBL-EBI's patent proteinsEMBL-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 filesGenBank'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/
  • HGNCCC0: https://www.genenames.org/about/license/
  • NCBI GeneNone 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 linksPublic domain (NIH RePORTER)
  • Open TargetsCC0 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
  • PubMedNLM's terms
  • PubTator 3Public domain
  • UniProtCC 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

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this gene from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/genes/v1/57532

GET https://conductscience.org/api/genes/v1/57532/patents