ConductScience.org, home

Gene · 26040

SETBP1: SET binding protein 1

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

Download JSON
Cite this record

ConductScience Library. SETBP1: SET binding protein 1. Genes, record 26040. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/26040

On this page

Gene

Symbol
SETBP1
HGNC
Name
SET binding protein 1
HGNC
NCBI Gene ID
26040
NCBI Gene
HGNC ID
HGNC:15573
HGNC
Ensembl
ENSG00000152217
NCBI Gene
Aliases
KIAA0437, MRD29, SEB
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
Q9Y6X0SET-binding protein1,5960Ensembl, GeneID, HGNC

Source UniProt

Patents25

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

PublicationPublishedSEQ ID NOProteinSource
JP 2026004568 A2026-01-1463285Q9Y6X0Espacenet
EP 4650780 A22025-11-1919606Q9Y6X0Espacenet
EP 4641201 A22025-10-2925356Q9Y6X0Espacenet
EP 4641202 A22025-10-299861Q9Y6X0Espacenet
JP 2025147176 A2025-10-0615606Q9Y6X0Espacenet
JP 2025517969 A2025-06-1225356Q9Y6X0Espacenet
JP 2025517970 A2025-06-1219606Q9Y6X0Espacenet
JP 2025032204 A2025-03-1135519Q9Y6X0Espacenet
JP 2025028160 A2025-02-2815606Q9Y6X0Espacenet
KR 1020250017231 A2025-02-049861Q9Y6X0Espacenet

1 to 10 of 25

See all 25 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 grants1,706

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

GrantTitleSETBP1 papersNewest fiscal year
P30CA016672Cancer Center Support Grant242025
P30CA008748Cancer Center Support Grant162025
P30CA016058Cancer Center Support Grant92025
R01MH101221Rare Mutations and Autism Spectrum Disorders82025
P30CA076292Moffitt Cancer Center Support Grant72025
U10CA180882Alliance Statistics and Data Management Center72025
P30CA006973Regional Oncology Research Center62025
P30CA015083Mayo Clinic Comprehensive Cancer Center Support Grant62025
P30CA082103Cancer Center Support Grant62025
P30DK063491Diabetes Research Center (DRC)62025

1 to 10 of 1,706Source NIH's project files

See all 1,706 nih grants

Papers2,649

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
Unravelling the genetic basis of stuttering: GWAS meta-analysis highlights link with rare speech disorders.medRxiv202642780237PubTator, text miningPubMed
Development of a human iPSC and patient phenotyping resource for preclinical investigations of neurodevelopmental disorders.Stem Cell Res202642612424PubTator, text miningPubMed
Clinical Characteristics and Diagnosis of Myelodysplastic Syndrome Accompanied by Eosinophilia and Basophilia.Clin Lab202642570659PubTator, text miningPubMed
Longitudinal Molecular Characterization of a Rare TPM3::PDGFRB-Rearranged Myeloid/Lymphoid Neoplasm With Late CNL-Like Neutrophilic Evolution.Eur J Haematol202642549531PubTator, text miningPubMed
Long-read, whole-genome sequencing and chemotherapy response of two patient-derived organoids from a TP53- and KRAS-mutant ovarian carcinoma.bioRxiv202642465424PubTator, text miningPubMed
Cumulative incidence and prognostic factors for leukemic transformation in chronic myelomonocytic leukemia: a competing risk analysis.BMC Cancer202642310629PubTator, text miningPubMed
Schinzel-Giedion Syndrome in One of Dizygotic Twins: Confirmation of a De Novo SET Binding Protein 1 (SETBP1) Variant and Classic Multisystem Phenotype.Cureus202642255817PubTator, text miningPubMed
[Correlation between Peripheral Blood Immunological Markers and Gene Mutations in Myelodysplastic Syndrome].Zhongguo Shi Yan Xue Ye Xue Za Zhi202642227435PubTator, text miningPubMed
[Clinical Characteristics and Prognosis Analysis of MDS-RS Patients with Wild-Type SF3B1].Zhongguo Shi Yan Xue Ye Xue Za Zhi202642227434PubTator, text miningPubMed
KATs in the MYST: A New Therapeutic Vulnerability for SETBP1-Mutated Myeloid Malignancies.Blood Cancer Discov202642223213PubTator, text miningPubMed

1 to 10 of 2,649

See all 2,649 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/v1/26040

GET https://conductscience.org/api/genes/v1/26040/patents?page=2