Gene · 8632
DNAH17: dynein axonemal heavy chain 17
12 sourcesgene-search-2026-11-11-0.2.0
Cite this record
ConductScience Library. DNAH17: dynein axonemal heavy chain 17. Genes, record 8632. Release gene-search-2026-11-11-0.2.0, 11 Nov 2026. https://conductscience.org/library/genes/8632
On this page
Gene
Proteins1
Reviewed human proteins whose Swiss-Prot entry states the gene.
| UniProt entry | Protein | Length | Structures | Gene stated in |
|---|---|---|---|---|
| Q9UFH2 | Dynein axonemal heavy chain 17 | 4,462 | 0 | Ensembl, GeneID, HGNC |
Source UniProt
Patents7
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 |
|---|---|---|---|---|
| EP 4641201 A2 | 2025-10-29 | 11132 | Q9UFH2 | Espacenet |
| JP 2025517969 A | 2025-06-12 | 11132 | Q9UFH2 | Espacenet |
| JP 2022141755 A | 2022-09-29 | 142 | Q9UFH2 | Espacenet |
| US 11446398 B2 | 2022-09-20 | 26075 | Q9UFH2 | Espacenet |
| JP 2022524081 A | 2022-04-27 | 129046 | Q9UFH2 | Espacenet |
| US 11078247 B2 | 2021-08-03 | 3140 | Q9UFH2 | Espacenet |
| JP 2016519285 A | 2016-06-30 | 142 | Q9UFH2 | Espacenet |
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 grants185
NIH grants whose papers are about the gene, through NIH's grant-paper links.
| Grant | Title | DNAH17 papers | Newest fiscal year |
|---|---|---|---|
| P20GM125503 | Center for Musculoskeletal Disease Research (CMDR) | 1 | 2025 |
| P30AG066515 | Stanford Alzheimer's Disease Research Center | 1 | 2025 |
| P30CA014051 | Cancer Center Support (Core) Grant | 1 | 2025 |
| P30CA021765 | Cancer Center Support Grant (CCSG) | 1 | 2025 |
| P30CA036727 | Buffett Cancer Center Support Grant | 1 | 2025 |
| P30CA068485 | Cancer Center Support Grant | 1 | 2025 |
| P30ES030285 | Gulf Coast Center for Precision Environmental Health | 1 | 2025 |
| P30EY008126 | Core Grant in Vision Research | 1 | 2025 |
| P50HD096723 | Genetics of Male Infertility: Accelerating the pace of discovery | 1 | 2025 |
| P51OD011092 | Support for National Primate Research Center | 1 | 2025 |
1 to 10 of 185Source NIH's project files
See all 185 nih grantsPapers285
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 |
|---|---|---|---|---|---|
| HIPK4 is a novel gene associated with teratozoospermia and male infertility. | Hum Reprod Open | 2026 | 42597842 | PubTator, text mining | PubMed |
| The potential role of dynein heavy chain genes in the pathophysiology of undescended testis. | Pediatr Surg Int | 2026 | 42323797 | PubTator, text mining | PubMed |
| A clinical protocol for the detection of comorbidities associated with monogenic causes of male infertility. | Hum Reprod | 2026 | 41863311 | PubTator, text mining | PubMed |
| Environmental and microbiome determinants of sperm quality: a narrative review on male health. | Transl Androl Urol | 2026 | 41809810 | 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 |
| PGVDA: a pathway-aggregated genetic dosage framework for interpretable disease classification using machine learning. | Brief Bioinform | 2026 | 41632594 | PubTator, text mining | PubMed |
| Novel homozygous or compound heterozygous DNAH17 variants lead to male infertility characterized by multiple morphological abnormalities of the sperm flagella and asthenoteratozoospermia in humans. | Asian J Androl | 2026 | 41549443 | PubTator, text mining | PubMed |
| Synolitic Graph Neural Networks of High-Dimensional Proteomic Data Enhance Early Detection of Ovarian Cancer. | Cancers (Basel) | 2025 | 41463217 | PubTator, text mining | PubMed |
| Novel DNAH17 Splice-Site Mutations Truncating the AAA6 Domain Cause Asthenozoospermia with MMAF. | Reprod Sci | 2025 | 41258988 | PubTator, text mining | PubMed |
| Identifying potential genetic biomarkers for sperm dysfunction through whole-genome sequencing. | Sci Rep | 2025 | 41115892 | PubTator, text mining | PubMed |
1 to 10 of 285
See all 285 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/v1/8632
GET https://conductscience.org/api/genes/v1/8632/grants?page=2