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Gene · 51684

SUFU: SUFU negative regulator of hedgehog signaling

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

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ConductScience Library. SUFU: SUFU negative regulator of hedgehog signaling. Genes, record 51684. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/51684

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Gene

Symbol
SUFU
HGNC
Name
SUFU negative regulator of hedgehog signaling
HGNC
NCBI Gene ID
51684
NCBI Gene
HGNC ID
HGNC:16466
HGNC
Ensembl
ENSG00000107882
NCBI Gene
Aliases
BCNS2, JBTS32, PRO1280, SUFUH, SUFUXL
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
Q9UMX1Suppressor of fused homolog48410Ensembl, GeneID, HGNC

Source UniProt

Patents37

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

PublicationPublishedSEQ ID NOProteinSource
EP 4650780 A22025-11-198689Q9UMX1Espacenet
JP 2025517970 A2025-06-128689Q9UMX1Espacenet
JP 2024123008 A2024-09-108585Q9UMX1Espacenet
WO 2023022218 A2023-02-2328Q9UMX1Espacenet
US 11446398 B22022-09-2085135Q9UMX1Espacenet
JP 2022537339 A2022-08-25128Q9UMX1Espacenet
JP 2022524081 A2022-04-27188106Q9UMX1Espacenet
US 10501513 B22019-12-108585Q9UMX1Espacenet
US 10330683 B22019-06-2510Q9UMX1Espacenet
JP 2019509721 A2019-04-115Q9UMX1Espacenet

1 to 10 of 37

See all 37 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 grants1,282

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

GrantTitleSUFU papersNewest fiscal year
P30CA021765Cancer Center Support Grant (CCSG)172025
R01CA159859Dysregulation of the Core Binding Factor Complex Inhibits Differentiation and Drives Group 4 Medulloblastoma172025
P30CA008748Cancer Center Support Grant152025
P30CA016672Cancer Center Support Grant152025
P01CA096832NORMAL & NEOPLASTIC GROWTH IN THE BRAIN132025
R35GM118063Cell signaling in development and regeneration102025
R01AR046786Stromal Regulation of Basal Cell Carcinoma Formation92025
UL1TR001863Yale Clinical and Translational Science Award82025
P30CA006973Regional Oncology Research Center72025
R35GM118082Signal transduction in development and disease52025

1 to 10 of 1,282Source NIH's project files

See all 1,282 nih grants

Papers2,311

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
Molecular profiling of pediatric medulloblastoma in Kazakhstan: Genomic alterations, subgroup distribution, and survival.Brain Pathol202642707049PubTator, text miningPubMed
Population-based genomic detection of childhood cancer predisposition using newborn dried blood spots.Nat Commun202642586985PubTator, text miningPubMed
Delayed Recognition of SUFU-Associated Gorlin Syndrome in a Renal Transplant Recipient.Dermatol Surg202642574229PubTator, text miningPubMed
PTCH1-Related Gorlin Syndrome: Expanding the Clinical and Molecular Spectrum in a Cohort of 11 Patients.Klin Padiatr202642462758PubTator, text miningPubMed
Mechanistic insights into transcriptional regulation of ARHGAP36 expression identify a factor predictive of neuroblastoma survival.Elife202642405753PubTator, text miningPubMed
Gorlin Syndrome: A Series of 10 Patients. Diagnosis, Follow-up, and Treatment from the Dermatological Consultation.Clin Exp Dermatol202642323190PubTator, text miningPubMed
JOSD1-mediated stabilization of SUFU controls pancreatic cancer progression.Cell Death Dis202642248831PubTator, text miningPubMed
Proteome-wide serology reveals immune-defined subtypes of gastrointestinal disease in systemic sclerosis.bioRxiv202642239272PubTator, text miningPubMed
Germline Predisposition in Pediatric Central Nervous System Tumors: Insights from a Multigene Panel Study.Oncol Res202642232602PubTator, text miningPubMed
Multi-Layered Genomic and Clinical Analysis Identifies Novel Variants, Co-Occurring Single Nucleotide Polymorphism Pairs, and Clinical Determinants of Host-Pathogen Interaction in COVID-19 Severity.J Med Virol202642198887PubTator, text miningPubMed

1 to 10 of 2,311

See all 2,311 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/v1/51684

GET https://conductscience.org/api/genes/v1/51684/patents?page=2