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Gene · 64072

CDH23: cadherin related 23

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

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ConductScience Library. CDH23: cadherin related 23. Genes, record 64072. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/64072

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Gene

Symbol
CDH23
HGNC
Name
cadherin related 23
HGNC
NCBI Gene ID
64072
NCBI Gene
HGNC ID
HGNC:13733
HGNC
Ensembl
ENSG00000107736
NCBI Gene
Aliases
CDHR23, DFNB12, PITA5, USH1D
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
Q9H251Cadherin-233,3546Ensembl, GeneID, HGNC

Source UniProt

Patents28

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

PublicationPublishedSEQ ID NOProteinSource
JP 2026515744 A2026-05-19177Q9H251Espacenet
EP 4650780 A22025-11-19612Q9H251Espacenet
EP 4640849 A22025-10-2972Q9H251Espacenet
EP 4641201 A22025-10-29430Q9H251Espacenet
EP 4641202 A22025-10-2921Q9H251Espacenet
EP 4641203 A22025-10-2917Q9H251Espacenet
JP 2025147176 A2025-10-062510Q9H251Espacenet
JP 2025529142 A2025-09-04867Q9H251Espacenet
JP 2025529142 A2025-09-045807Q9H251Espacenet
US 12371689 B22025-07-295807Q9H251Espacenet

1 to 10 of 28

See all 28 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 grants1,030

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

GrantTitleCDH23 papersNewest fiscal year
R01DC012049Optimizing Genetic Testing for Deafness for Clinical Diagnostics212025
ZIADC000039Identification of Genes Causing Syndromic and Nonsyndromic Hearing Impairment122025
R01DC003594Identification of Autosomal Recessive Nonsyndromic Hearing Impairment Genes92025
ZIADC000048Functional Studies of "Deafness Genes" Essential for Hearing72025
P50DC000422Experimental and Clinical Studies of Presbyacusis Extension and Supplement62025
R01DC009645A Collaborative Search for New Genes for Non-Syndromic Deafness62025
R01DC012564Usher Proteins in the Inner ear Structure and Function62025
R01DC015271Nanomechanics of inner-ear hair-cell transduction62025
R01DK095811Molecular basis of brush border assembly62025
ZIADC000002Structural and Molecular Basis of Transduction in Auditory Sensory Organs62025

1 to 10 of 1,030Source NIH's project files

See all 1,030 nih grants

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.

TitleJournalYearPMIDFound bySource
STOML1 as an Exploratory Candidate Gene for Autosomal Dominant Iris and Chorioretinal Coloboma in a British Family.Genes (Basel)202642793046PubTator, text miningPubMed
Mutation Spectrum and Novel Rare Variants in a Han Chinese Hearing Loss Cohort Using a Tiered Sequencing Strategy.Mol Genet Genomic Med202642764263PubTator, text miningPubMed
Two Novel Compound Heterozygous CDH23 Mutations Underlying Non-Syndromic Hearing Loss.Int J Gen Med202642657335PubTator, text miningPubMed
New insights into the complex genetic architecture of age-related hearing loss.Eur J Med Genet202642379497PubTator, text miningPubMed
Cryo-EM reveals a right-handed double-helix dimer architecture of PCDH15.Proc Natl Acad Sci U S A202642263124PubTator, text miningPubMed
Identification of candidate genes for keratoconus by trio-based whole-exome sequencing in 81 families from Northwest China.Exp Eye Res202642162727PubTator, text miningPubMed
The germline landscape of pituitary adenomas: established and emerging predisposition genes.J Clin Endocrinol Metab202642141904PubTator, text miningPubMed
Bilateral retinal astrocytic hamartomas in retinitis pigmentosa: two case reports and systematic review.Doc Ophthalmol202642133270PubTator, text miningPubMed
Genetic studies identify known and novel variants for recessively inherited moderate to severe hearing loss in consanguineous families from Pakistan.Sci Rep202642086625PubTator, text miningPubMed
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 Sci202641893653PubTator, text miningPubMed

1 to 10 of 1,428

See all 1,428 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/v1/64072

GET https://conductscience.org/api/genes/v1/64072/patents?page=2