Evidence map›Paper›PMID 36305828›Full record

ArticleNucleic acids research2023

The new uORFdb: integrating literature, sequence, and variation data in a central hub for uORF research.

Felix Manske, Lynn Ogoniak, Lara Jürgens, Norbert Grundmann, Wojciech Makałowski, Klaus Wethmar

Open access · goldAbstract read
In one paragraph

Article in Nucleic acids research, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
2.9field-weighted citation impact, top 8% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 36 citations in OpenAlex.

  1. Functional analysis ofMolecular therapy. Nucleic acids · 2026
    Article
  2. Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Article
  8. Non-coding single-nucleotide and structural variants affecting the EYS putative promoter cause autosomal recessive retinitis pigmentosa.Genetics in medicine : official journal of the American College of Medical Genetics · 2025
    Article
  9. Article
  10. Decoding meLife · 2025
    Article
  11. Decoding mbioRxiv : the preprint server for biology · 2025
    Article
  12. Article
  13. Article
  14. CytosolicProceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Felix ManskeInstitute of Bioinformatics, University of Münster, Münster 48149, Germany.ORCID 0000-0001-6509-2063
Lynn OgoniakInstitute of Bioinformatics, University of Münster, Münster 48149, Germany.ORCID 0000-0002-2739-0251
Lara JürgensDepartment of Medicine A, Hematology, Oncology, Hemostaseology and Pneumology, University Hospital Münster, Münster 48149, Germany.ORCID 0000-0001-6910-8341
Norbert GrundmannInstitute of Bioinformatics, University of Münster, Münster 48149, Germany.ORCID 0000-0001-8743-2348
Wojciech MakałowskiInstitute of Bioinformatics, University of Münster, Münster 48149, Germany.ORCID 0000-0003-2303-9541
Klaus WethmarDepartment of Medicine A, Hematology, Oncology, Hemostaseology and Pneumology, University Hospital Münster, Münster 48149, Germany.ORCID 0000-0002-1899-3261
University of Münster · DEUniversity Hospital Münster · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Upstream open reading frames (uORFs) are initiated by AUG or near-cognate start codons and have been identified in the transcript leader sequences of the majority of eukaryotic transcripts. Functionally, uORFs are implicated in downstream translational regulation of the main protein coding sequence and may serve as a source of non-canonical peptides. Genetic defects in uORF sequences have been linked to the development of various diseases, including cancer. To simplify uORF-related research, the initial release of uORFdb in 2014 provided a comprehensive and manually curated collection of uORF-related literature. Here, we present an updated sequence-based version of uORFdb, accessible at https://www.bioinformatics.uni-muenster.de/tools/uorfdb. The new uORFdb enables users to directly access sequence information, graphical displays, and genetic variation data for over 2.4 million human uORFs. It also includes sequence data of >4.2 million uORFs in 12 additional species. Multiple uORFs can be displayed in transcript- and reading-frame-specific models to visualize the translational context. A variety of filters, sequence-related information, and links to external resources (UCSC Genome Browser, dbSNP, ClinVar) facilitate immediate in-depth analysis of individual uORFs. The database also contains uORF-related somatic variation data obtained from whole-genome sequencing (WGS) analyses of 677 cancer samples collected by the TCGA consortium.

Indexed as

Databases, GeneticOpen Reading Frames5' Untranslated RegionsCodon, InitiatorEukaryotaHumansNeoplasmsProtein Biosynthesis5' Untranslated RegionsCodon, Initiator

Identifiers

PMID36305828
PMCPMC9825577
OpenAlexW4307468144

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.