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Gene · 6311

ATXN2: ataxin 2

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

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ConductScience Library. ATXN2: ataxin 2. Genes, record 6311. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/6311

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Gene

Symbol
ATXN2
HGNC
Name
ataxin 2
HGNC
NCBI Gene ID
6311
NCBI Gene
HGNC ID
HGNC:10555
HGNC
Ensembl
ENSG00000204842
NCBI Gene
Aliases
ATX2, SCA2, TNRC13
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
Q99700Ataxin-21,3131Ensembl, GeneID, HGNC

Source UniProt

Patents19

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

PublicationPublishedSEQ ID NOProteinSource
JP 2026004568 A2026-01-1438049Q99700Espacenet
EP 4640849 A22025-10-293158Q99700Espacenet
EP 4641201 A22025-10-2920245Q99700Espacenet
JP 2025519096 A2025-06-243158Q99700Espacenet
JP 2025517969 A2025-06-1220245Q99700Espacenet
JP 2025062604 A2025-04-146859Q99700Espacenet
JP 2025062604 A2025-04-146865Q99700Espacenet
JP 2024045131 A2024-04-028Q99700Espacenet
US 11446398 B22022-09-206859Q99700Espacenet
US 11446398 B22022-09-206865Q99700Espacenet

1 to 10 of 19

See all 19 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 grants2,368

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

GrantTitleATXN2 papersNewest fiscal year
P30DK063491Diabetes Research Center (DRC)162025
R01HL086694From GWAS loci to blood pressure genes, variants & mechanisms - Renewal112025
P01AG019724Frontotemporal Dementia: Genes, Images, and Emotions102025
R01EY022305NEIGHBORHOOD Consortium for POAG Genetics102025
P30EY014104P30 Core Grant for Vision Research82025
UL1TR001881UCLA Clinical and Translational Science Institute82025
P30ES009089Center for Environmental Health in Northern Manhattan72025
R01NS124854Targeting Cerebellar Endoplasmic Reticulum Calcium Handling in Essential Tremor72025
P40OD018537Bloomington Drosophila Stock Center at Indiana University62025
ZIAAG000933Genetic etiology of Amyotrophic Lateral Sclerosis62025

1 to 10 of 2,368Source NIH's project files

See all 2,368 nih grants

Papers3,217

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
Large-scale genetic profiling of hereditary ataxias in China: implications for a stepwise molecular diagnostic strategy.Transl Neurodegener202642806408PubTator, text miningPubMed
Hereditary and Non-hereditary Cerebellar Ataxias in Latvia: Six Years of Experience at the National Reference Centre (ERN-RND Affiliated Partner).Cerebellum202642802208PubTator, text miningPubMed
Genetics of Celiac Disease in Southern Brazil: High-Resolution HLA Haplotypes and Non-HLA Polymorphisms.HLA202642798292PubTator, text miningPubMed
Unified long-read panel for Parkinson's and repeat expansion disorders.NPJ Parkinsons Dis202642786195PubTator, text miningPubMed
An ATXN2-linked stress granule transcript program marks proliferative and CD8-low states in colorectal cancer.Comput Biol Chem202642777445PubTator, text miningPubMed
CRISPR-based functional genomic screening in neurodegeneration: mechanistic insights into AD, PD, and ALS.Front Aging Neurosci202642775169PubTator, text miningPubMed
The bioinformatics approach to identifying pathogenic variants for colorectal cancer (CRC).J Genet Eng Biotechnol202642749394PubTator, text miningPubMed
ABCD1-Related Disease Presenting as an Upper Motor Neuron-Predominant Amyotrophic Lateral Sclerosis Mimic in a Colombian Female Heterozygote: A Case Report.Cureus202642746497PubTator, text miningPubMed
Predicting disease progression in progressive cerebellar ataxias: integrating clinical, imaging, fluid, genetic, and digital biomarkers.Front Neurol202642677125PubTator, text miningPubMed
ATXN2 Spectrum Disorders: Genetic Complexity Beyond Dominant Inheritance.Neurol Genet202642666931PubTator, text miningPubMed

1 to 10 of 3,217

See all 3,217 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/v1/6311

GET https://conductscience.org/api/genes/v1/6311/patents