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Gene · 51119

SBDS: SBDS ribosome maturation factor

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

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ConductScience Library. SBDS: SBDS ribosome maturation factor. Genes, record 51119. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/51119

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Gene

Symbol
SBDS
HGNC
Name
SBDS ribosome maturation factor
HGNC
NCBI Gene ID
51119
NCBI Gene
HGNC ID
HGNC:19440
HGNC
Ensembl
ENSG00000126524
NCBI Gene
Aliases
CGI-97, FLJ10917, SDO1, SDS, SWDS
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
Q9Y3A5Ribosome maturation protein SBDS2506Ensembl, GeneID, HGNC

Source UniProt

Patents34

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

PublicationPublishedSEQ ID NOProteinSource
JP 2026004568 A2026-01-1463487Q9Y3A5Espacenet
JP 2025183226 A2025-12-1662Q9Y3A5Espacenet
EP 4650780 A22025-11-191203Q9Y3A5Espacenet
EP 4641201 A22025-10-29854Q9Y3A5Espacenet
JP 2025517969 A2025-06-12854Q9Y3A5Espacenet
JP 2025517970 A2025-06-121203Q9Y3A5Espacenet
JP 2025032204 A2025-03-1135232Q9Y3A5Espacenet
EP 4461818 A22024-11-1335232Q9Y3A5Espacenet
JP 2023058610 A2023-04-2535232Q9Y3A5Espacenet
JP 2022545950 A2022-11-0197Q9Y3A5Espacenet

1 to 10 of 34

See all 34 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 grants465

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

GrantTitleSBDS papersNewest fiscal year
ZIACP010144Clinical Genetic Studies of Familial and Hereditary Cancer Syndromes62025
P30CA015704Cancer Center Support Grant52025
R01DK132812Genetic Dissection of Stress Responses in Shwachman-Diamond Syndrome52025
T32HL007574Pathophysiology of Human Blood Cells52025
K12HD028827Child Health Research Career Development Award (K1-Renewal Yrs 31-35)42025
U01DK108334INSPPIRE: Using the natural history of pediatric chronic pancreatitis to identify disease predictors and design therapies42025
P30CA008748Cancer Center Support Grant32025
R35GM131687Novel regulatory networks driving human ribosome biogenesis32025
P30CA006973Regional Oncology Research Center22025
P30CA125123Baylor College of Medicine Cancer Center - Cancer Center Support Grant22025

1 to 10 of 465Source NIH's project files

See all 465 nih grants

Papers775

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
Genetic Heterogeneity of Inborn Errors of Immunity Revealed by Whole-Genome Sequencing: Insights from a Russian Patient Cohort.Int J Mol Sci202642737820PubTator, text miningPubMed
Genetic variant profile in a cohort of inherited bone marrow failure patients from North india.Indian J Hematol Blood Transfus202642712617PubTator, text miningPubMed
Analysing long-read CRISPR experiments with CRISPRLungo.Nat Biomed Eng202642624993PubTator, text miningPubMed
Neurovascular-Immune Biomarkers in Ménière Disease: Insights From High-Throughput Proteomics.Otol Neurotol202642584982PubTator, text miningPubMed
A Multi-omics and Machine Learning Framework Identifies Plasma SBDS as a Causal Biomarker and Therapeutic Target in Primary Sclerosing Cholangitis.J Clin Transl Hepatol202642483734PubTator, text miningPubMed
Generation of iPSC and isogenic gene-corrected lines from a patient with Shwachman Diamond syndrome.Stem Cell Res202642364508PubTator, text miningPubMed
Pancreatitis Risk Genes Play a Major Role in Pediatric Pancreatitis: Insights From the INternational Study Group of Pediatric Pancreatitis: In search for a cuRE.Clin Gastroenterol Hepatol202642303027PubTator, text miningPubMed
Beyond neutropenia: Immunological evaluation of patients with Shwachman-Diamond syndrome.Br J Haematol202642185746PubTator, text miningPubMed
Congenital Temporomandibular Joint Ankylosis: Investigating Potential Genetic Etiologies with Whole Exome Sequencing.J Clin Med202641753091PubTator, text miningPubMed
Phenotypic Variability Associated with Jagunal Homolog 1 (JAGN1) Deficiency Caused by the c.63G>T Variant.Int J Mol Sci202641751872PubTator, text miningPubMed

1 to 10 of 775

See all 775 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/v1/51119

GET https://conductscience.org/api/genes/v1/51119/patents?page=2