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Gene · 4647

MYO7A: myosin VIIA

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

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ConductScience Library. MYO7A: myosin VIIA. Genes, record 4647. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/4647

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Gene

Symbol
MYO7A
HGNC
Name
myosin VIIA
HGNC
NCBI Gene ID
4647
NCBI Gene
HGNC ID
HGNC:7606
HGNC
Ensembl
ENSG00000137474
NCBI Gene
Aliases
DFNA11, DFNB2, MYOVIIA, MYU7A, NSRD2, USH1B
NCBI Gene
Type
protein-coding
NCBI Gene

Proteins1

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

UniProt entryProteinLengthStructuresGene stated in
Q13402Unconventional myosin-VIIa2,2151Ensembl, GeneID, HGNC

Source UniProt

Patents35

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

PublicationPublishedSEQ ID NOProteinSource
JP 2026515744 A2026-05-19202Q13402Espacenet
EP 4731771 A12026-04-2962Q13402Espacenet
EP 4704920 A12026-03-11201Q13402Espacenet
JP 2026004568 A2026-01-1454661Q13402Espacenet
EP 4641201 A22025-10-2912922Q13402Espacenet
WO 2025153705 A12025-07-24135Q13402Espacenet
WO 2025153705 A12025-07-2415Q13402Espacenet
JP 2025517969 A2025-06-1212922Q13402Espacenet
EP 4551703 A22025-05-1431Q13402Espacenet
JP 2025032204 A2025-03-1131979Q13402Espacenet

1 to 10 of 35

See all 35 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 grants1,077

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

GrantTitleMYO7A papersNewest fiscal year
R01DC012049Optimizing Genetic Testing for Deafness for Clinical Diagnostics252025
ZIADC000039Identification of Genes Causing Syndromic and Nonsyndromic Hearing Impairment202025
R01DC003594Identification of Autosomal Recessive Nonsyndromic Hearing Impairment Genes132025
ZIADC000048Functional Studies of "Deafness Genes" Essential for Hearing122025
P30EY000331Vision Research Core at UCLA112025
R01DC009645A Collaborative Search for New Genes for Non-Syndromic Deafness102025
R01DC012564Usher Proteins in the Inner ear Structure and Function92025
P30DK058404Molecular and Cellular Basis for Digestive Diseases82025
R01DK095811Molecular basis of brush border assembly72025
ZIADC000002Structural and Molecular Basis of Transduction in Auditory Sensory Organs72025

1 to 10 of 1,077Source NIH's project files

See all 1,077 nih grants

Papers1,877

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
Early Molecular Testing for Presumptive Genetic Eye Diseases.Genes (Basel)202642792986PubTator, text miningPubMed
Timing and Dosage of Notch Inhibition and Wnt Activation Enhanced Hair Cell-Like Cell Generation and Stereocilia Elongation in Otic Organoids.Stem Cells Dev202642788198PubTator, text miningPubMed
Otoprotective effect of MnTBAP in cisplatin-induced hearing loss.PLoS One202642766579PubTator, text miningPubMed
Mesenchymal drift in ciliopathy iPSC-derived RPE reveals a convergent pathogenic cell state.Cell Rep202642667617PubTator, text miningPubMed
Whole exome sequencing of paediatric patients with Cogan's syndrome to identify monogenic mimics.Rheumatology (Oxford)202642640550PubTator, text miningPubMed
Genetic contributions to familial Ménière's disease: a systematic review.Eur Arch Otorhinolaryngol202642625013PubTator, text miningPubMed
Compound heterozygous splicing and missense variants in MYO7A in a Chinese patient with Usher syndrome.Front Med (Lausanne)202642569614PubTator, text miningPubMed
Increased Adrenergic Receptor Expression in Meniere Disease.Otol Neurotol202642531530PubTator, text miningPubMed
New insights into the complex genetic architecture of age-related hearing loss.Eur J Med Genet202642379497PubTator, text miningPubMed
Clinical manifestations of dual-gene variants in retinitis pigmentosa.Acta Ophthalmol202642360046PubTator, text miningPubMed

1 to 10 of 1,877

See all 1,877 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/v1/4647

GET https://conductscience.org/api/genes/v1/4647/patents?page=2