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Gene · 5962

RDX: radixin

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

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ConductScience Library. RDX: radixin. Genes, record 5962. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/5962

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Gene

Symbol
RDX
HGNC
Name
radixin
HGNC
NCBI Gene ID
5962
NCBI Gene
HGNC ID
HGNC:9944
HGNC
Ensembl
ENSG00000137710
NCBI Gene
Aliases
DFNB24
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
P35241Radixin5832Ensembl, GeneID, HGNC

Source UniProt

Patents51

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

PublicationPublishedSEQ ID NOProteinSource
EP 4650780 A22025-11-1919533P35241Espacenet
EP 4641201 A22025-10-2925144P35241Espacenet
JP 2025517969 A2025-06-1225144P35241Espacenet
JP 2025517970 A2025-06-1219533P35241Espacenet
JP 2024123008 A2024-09-108049P35241Espacenet
JP 2024510010 A2024-03-05178P35241Espacenet
WO 2022195543 A2022-09-22178P35241Espacenet
US 11446398 B22022-09-2071257P35241Espacenet
JP 2022524081 A2022-04-27174228P35241Espacenet
US 10857244 B22020-12-08105P35241Espacenet

1 to 10 of 51

See all 51 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 grants2,051

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

GrantTitleRDX papersNewest fiscal year
P30CA016672Cancer Center Support Grant162025
P01CA097132Sphingolipids in Cancer Biology and Therapy72025
P30CA068485Cancer Center Support Grant72025
P30CA008748Cancer Center Support Grant62025
P30DK058404Molecular and Cellular Basis for Digestive Diseases62025
P30CA006973Regional Oncology Research Center52025
ZIAAR041159Cytokine Signaling, Immunoregulation and Autoimmune and Immunodeficiency Diseases52025
P30CA006927Comprehensive Cancer Center Program at Fox Chase42025
ZIADC000039Identification of Genes Causing Syndromic and Nonsyndromic Hearing Impairment42025
P01AI063302The intersection of innate and adaptive immunity to intracellular pathogens32025

1 to 10 of 2,051Source NIH's project files

See all 2,051 nih grants

Papers3,092

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
MATR3 is essential for oocyte growth and maturation quality through a dual molecular mechanism.Elife202642765984PubTator, text miningPubMed
Betulonic acid, a bioactive triterpenoid from Celastrus orbiculatus extract, reverses chemoresistance in gastric cancer via CD44v6-mediated actin cytoskeleton remodeling.Phytomedicine202642759326PubTator, text miningPubMed
Growth factor receptor corralling fuels persistent leader-bleb dynamics.Dev Cell202642715994PubTator, text miningPubMed
Altered Placental Ezrin Expression in Gestational Diabetes Mellitus: An Immunohistochemical and Bioinformatic Analysis.Diagnostics (Basel)202642587641PubTator, text miningPubMed
CRISPR activation screen uncovers MARCKSL1 as a gauge for extracellular vesicle secretion.Cell Rep202642536484PubTator, text miningPubMed
TRPML1 positions lysosomes and regulates actin-membrane linkers in astrocyte processes.bioRxiv202642395471PubTator, text miningPubMed
Cochlear implantation in a child with biallelic RDX variant (DFNB24): long-term auditory outcome.Acta Otorrinolaringol Esp (Engl Ed)202642392404PubTator, text miningPubMed
The Impact of Zinc on T Cell Motility and the Immunological Synapse.Int J Mol Sci202642352977PubTator, text miningPubMed
Rho-associated coiled-coil-containing protein kinase signaling preserves alveolar type II cell identity by antagonizing transforming growth factor-β1-driven epithelial remodeling in idiopathic pulmonary fibrosis.
Exp Mol Pathol202642096940PubTator, text miningPubMed
Astrocyte targeted SMN1 gene therapy and forskolin application improves astrocyte filopodia actin defects and motor neuron synaptic dysfunction in human SMA disease pathology.bioRxiv202641929212PubTator, text miningPubMed

1 to 10 of 3,092

See all 3,092 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/v1/5962

GET https://conductscience.org/api/genes/v1/5962/patents?page=2