Gene · 64072
Papers1,428
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
1 to 20 of 1,428
Download this page as JSON| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| STOML1 as an Exploratory Candidate Gene for Autosomal Dominant Iris and Chorioretinal Coloboma in a British Family. | Genes (Basel) | 2026 | 42793046 | PubTator, text mining | PubMed |
| Mutation Spectrum and Novel Rare Variants in a Han Chinese Hearing Loss Cohort Using a Tiered Sequencing Strategy. | Mol Genet Genomic Med | 2026 | 42764263 | PubTator, text mining | PubMed |
| Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss. | Int J Gen Med | 2026 | 42657335 | PubTator, text mining | PubMed |
| New insights into the complex genetic architecture of age-related hearing loss. | Eur J Med Genet | 2026 | 42379497 | PubTator, text mining | PubMed |
| Cryo-EM reveals a right-handed double-helix dimer architecture of PCDH15. | Proc Natl Acad Sci U S A | 2026 | 42263124 | PubTator, text mining | PubMed |
| Identification of candidate genes for keratoconus by trio-based whole-exome sequencing in 81 families from Northwest China. | Exp Eye Res | 2026 | 42162727 | PubTator, text mining | PubMed |
| The germline landscape of pituitary adenomas: established and emerging predisposition genes. | J Clin Endocrinol Metab | 2026 | 42141904 | PubTator, text mining | PubMed |
| Bilateral retinal astrocytic hamartomas in retinitis pigmentosa: two case reports and systematic review. | Doc Ophthalmol | 2026 | 42133270 | PubTator, text mining | PubMed |
| Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from Pakistan. | Sci Rep | 2026 | 42086625 | PubTator, text mining | PubMed |
| African Swine Fever Virus R238L and R298L Disrupt Lung Cell Collagen Formation and Cell Adhesion Pathway by Targeting Transcription Factors Containing zf-C2H2 Domain. | Vet Sci | 2026 | 41893653 | PubTator, text mining | PubMed |
| Genetic epidemiology of Moroccan pediatric cochlear implantation patients. | Acta Otolaryngol | 2026 | 41889064 | PubTator, text mining | PubMed |
| Cryo-EM reveals a right-handed double-helix dimer architecture of PCDH15 critical for mechanotransduction. | bioRxiv | 2026 | 41846998 | PubTator, text mining | PubMed |
| Vestibular function prior to cochlear implantation in patients with non-syndromic hearing loss caused by CDH23 mutations: a retrospective case series. | Acta Otolaryngol | 2026 | 41821471 | PubTator, text mining | PubMed |
| Homozygous Myo7A mutation associations teratozoospermia and intracytoplasmic sperm injection failure in humans and mice. | Transl Androl Urol | 2026 | 41809782 | PubTator, text mining | PubMed |
| Alteplase and Angioedema: Can Clinical Exome Sequencing Redefine the Paradigm? | Life (Basel) | 2026 | 41752838 | PubTator, text mining | PubMed |
| Abnormal Hearing Phenotypes in "Ignorome" Knockout Mice as Predictors of Cognitive Dysfunction. | Genes Brain Behav | 2026 | 41738368 | PubTator, text mining | PubMed |
| ATP8B1-TMEM30B Flippase Activity Maintains Stereocilia Lipid Asymmetry Required for Hearing. | bioRxiv | 2026 | 41726979 | PubTator, text mining | PubMed |
| Cadherin-23 mutations cause calcium-dependent, allele-sensitive mechanosensory defects. | iScience | 2026 | 41716990 | PubTator, text mining | PubMed |
| CDH23-associated Usher syndrome: genotype-phenotype correlations. | Ophthalmic Genet | 2026 | 41709431 | PubTator, text mining | PubMed |
| ELOC-mutated Renal Cell Carcinoma: Clinicopathologic, Immunohistochemical, and Molecular Genetic Analysis of 35 Cases. | Mod Pathol | 2026 | 41690476 | PubTator, text mining | PubMed |
gene-search-2026-11-11-0.2.0
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.
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