Gene · 4647
MYO7A: myosin VIIA
12 sourcesgene-search-2026-11-11-0.2.0
Cite this record
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
On this page
Gene
Proteins1
Reviewed human proteins whose Swiss-Prot entry states the gene.
| UniProt entry | Protein | Length | Structures | Gene stated in |
|---|---|---|---|---|
| Q13402 | Unconventional myosin-VIIa | 2,215 | 1 | Ensembl, GeneID, HGNC |
Source UniProt
Patents35
Patents whose sequence listing contains this protein's exact sequence. A patent can list a sequence without claiming it.
| Publication | Published | SEQ ID NO | Protein | Source |
|---|---|---|---|---|
| JP 2026515744 A | 2026-05-19 | 202 | Q13402 | Espacenet |
| EP 4731771 A1 | 2026-04-29 | 62 | Q13402 | Espacenet |
| EP 4704920 A1 | 2026-03-11 | 201 | Q13402 | Espacenet |
| JP 2026004568 A | 2026-01-14 | 54661 | Q13402 | Espacenet |
| EP 4641201 A2 | 2025-10-29 | 12922 | Q13402 | Espacenet |
| WO 2025153705 A1 | 2025-07-24 | 135 | Q13402 | Espacenet |
| WO 2025153705 A1 | 2025-07-24 | 15 | Q13402 | Espacenet |
| JP 2025517969 A | 2025-06-12 | 12922 | Q13402 | Espacenet |
| EP 4551703 A2 | 2025-05-14 | 31 | Q13402 | Espacenet |
| JP 2025032204 A | 2025-03-11 | 31979 | Q13402 | Espacenet |
1 to 10 of 35
See all 35 patentsDrugs0
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.
| Grant | Title | MYO7A papers | Newest fiscal year |
|---|---|---|---|
| R01DC012049 | Optimizing Genetic Testing for Deafness for Clinical Diagnostics | 25 | 2025 |
| ZIADC000039 | Identification of Genes Causing Syndromic and Nonsyndromic Hearing Impairment | 20 | 2025 |
| R01DC003594 | Identification of Autosomal Recessive Nonsyndromic Hearing Impairment Genes | 13 | 2025 |
| ZIADC000048 | Functional Studies of "Deafness Genes" Essential for Hearing | 12 | 2025 |
| P30EY000331 | Vision Research Core at UCLA | 11 | 2025 |
| R01DC009645 | A Collaborative Search for New Genes for Non-Syndromic Deafness | 10 | 2025 |
| R01DC012564 | Usher Proteins in the Inner ear Structure and Function | 9 | 2025 |
| P30DK058404 | Molecular and Cellular Basis for Digestive Diseases | 8 | 2025 |
| R01DK095811 | Molecular basis of brush border assembly | 7 | 2025 |
| ZIADC000002 | Structural and Molecular Basis of Transduction in Auditory Sensory Organs | 7 | 2025 |
1 to 10 of 1,077Source NIH's project files
See all 1,077 nih grantsPapers1,877
Newest first. Swiss-Prot's references are curated; PubTator's text mining finds papers that name the gene, not always ones about it.
| Title | Journal | Year | PMID | Found by | Source |
|---|---|---|---|---|---|
| Early Molecular Testing for Presumptive Genetic Eye Diseases. | Genes (Basel) | 2026 | 42792986 | PubTator, text mining | PubMed |
| Timing and Dosage of Notch Inhibition and Wnt Activation Enhanced Hair Cell-Like Cell Generation and Stereocilia Elongation in Otic Organoids. | Stem Cells Dev | 2026 | 42788198 | PubTator, text mining | PubMed |
| Otoprotective effect of MnTBAP in cisplatin-induced hearing loss. | PLoS One | 2026 | 42766579 | PubTator, text mining | PubMed |
| Mesenchymal drift in ciliopathy iPSC-derived RPE reveals a convergent pathogenic cell state. | Cell Rep | 2026 | 42667617 | PubTator, text mining | PubMed |
| Whole exome sequencing of paediatric patients with Cogan's syndrome to identify monogenic mimics. | Rheumatology (Oxford) | 2026 | 42640550 | PubTator, text mining | PubMed |
| Genetic contributions to familial Ménière's disease: a systematic review. | Eur Arch Otorhinolaryngol | 2026 | 42625013 | PubTator, text mining | PubMed |
| Compound heterozygous splicing and missense variants in MYO7A in a Chinese patient with Usher syndrome. | Front Med (Lausanne) | 2026 | 42569614 | PubTator, text mining | PubMed |
| Increased Adrenergic Receptor Expression in Meniere Disease. | Otol Neurotol | 2026 | 42531530 | 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 |
| Clinical manifestations of dual-gene variants in retinitis pigmentosa. | Acta Ophthalmol | 2026 | 42360046 | PubTator, text mining | PubMed |
1 to 10 of 1,877
See all 1,877 papersSources 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