Logo
Homepage
Explore Our Models
My Cart
Contact
Subscribe
Models
Genetically Engineered Animals
Knockout Mice
Knockout Rats
Knockin Mice
Knockin Rats
Transgenic Mice
Transgenic Rats
Model Generation Techniques
Turboknockout<sup>®</sup> Gene Targeting
ES Cell Gene Targeting
Targeted Gene Editing
Regular Transgenic
PiggyBac Transgenesis
BAC Transgenic
Research Models
HUGO-GT™ Humanized Mice
Cre Mouse Lines
Humanized Target Gene Models
Metabolic Disease Models
Ophthalmic Disease Models
Neurological Disease Models
Autoimmune Disease Models
Immunodeficient Mouse Models
Humanized Immune System Mouse Models
Oncology & Immuno-oncology Models
Covid-19 Mouse Models
MouseAtlas Model Library
Knockout Cell Line Product Catalog
Tumor Cell Line Product Catalog
AAV Standard Product Catalog
Animal Supporting Services
Breeding Services
Cryopreservation & Recovery
Phenotyping Services
BAC Modification
Custom Cell Line Models
Induced Pluripotent Stem Cells (iPSCs)
Knockout Cell Lines
Knockin Cell Lines
Point Mutation Cell Lines
Overexpression Cell Lines
Virus Packaging
Adeno-associated Virus (AAV) Packaging
Lentivirus Packaging
Adenovirus Packaging
CRO Services
By Therapeutic Area
Oncology
Ophthalmology
Neuroscience
Metabolic & Cardiovascular Diseases
Autoimmune & Inflammatory
By Drug Type
AI-Powered AAV Discovery
Gene Therapy
Oligonucleotide Therapy
Antibody Therapy
Cell Immunotherapy
Resources
Promotion
Events & Webinars
Newsroom
Blogs & Insights
Resource Vault
Reference Databases
Peer-Reviewed Citations
Rare Disease Data Center
AbSeek
Cell iGeneEditor™ System
OriCell
Quality
Facility Overview
Animal Health & Welfare
Health Reports
About Us
Corporate Overview
Our Partners
Careers
Contact Us
Login
Request a Product Quote
Select products from our catalogs and submit your request. Our team will get back to you with detailed information.
Full Name
Email
Phone Number
Organization
Job Role
Country
Catalog Type
Product Name
Additional Comments
Cyagen values your privacy. We’d like to keep you informed about our latest offerings and insights. Your preferences:
You may unsubscribe from these communications at any time. See our Privacy Policy for details on opting out and data protection.
By clicking the button below, you consent to allow Cyagen to store and process the personal information submitted in this form to provide you the content requested.
C57BL/6JCya-Zcwpw1em1flox/Cya
Common Name:
Zcwpw1-flox
Product ID:
S-CKO-19222
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
Price:
Contact for Pricing
Basic Information
Strain Name
Zcwpw1-flox
Strain ID
CKOCMP-381678-Zcwpw1-B6J-VB
Gene Name
Zcwpw1
Product ID
S-CKO-19222
Gene Alias
Gm1053
Background
C57BL/6JCya
NCBI ID
381678
Modification
Conditional knockout
Chromosome
5
Phenotype
MGI:2685899
Document
Click here to download >>
Application
--
More
Rare Disease Data Center >>
Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Zcwpw1em1flox/Cya mice (Catalog S-CKO-19222) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000035852
NCBI RefSeq
NM_001005426
Target Region
Exon 3
Size of Effective Region
~1.6 kb
Detailed Document
Click here to download >>
Overview of Gene Research
Zcwpw1, with no common aliases provided, is an essential factor in meiotic processes. It is recruited to recombination hotspots by PRDM9 and plays a crucial role in meiotic double-strand break repair, which is vital for homologous chromosomes to pair and recombine, ensuring balanced segregation and genetic diversity in sexual reproduction [1,2,4,5,7]. This process is integral to the formation of sex cells.

Male Zcwpw1 knockout mice show severe DSB repair and synapsis defects, leading to sterility. Their spermatocytes are arrested at the pachytene-like stage, phenocopying the knockout mice. In contrast, in female mice, deletion of Zcwpw1 only slows down meiosis prophase I progression, and they can still maintain normal fertility until mid-adulthood [1,2,4]. A loss-of-function variant in ZCWPW1 in humans has also been reported to cause male infertility with sperm head defect and high DNA fragmentation [6]. Additionally, Zcwpw1 has been associated with Alzheimer's disease risk, as rare-variant burden in it highlighted this gene as a potential driver of an AD-genome-wide association study locus [3].

In conclusion, Zcwpw1 is indispensable for meiotic synapsis in males, playing a key role in the production of male sex cells. Mouse knockout models have been instrumental in revealing its role in male fertility. Its association with Alzheimer's disease also indicates its potential importance in neurodegenerative disease research, although further study is needed to fully understand this connection.

References:
1. Wells, Daniel, Bitoun, Emmanuelle, Moralli, Daniela, Green, Catherine, Myers, Simon R. 2020. ZCWPW1 is recruited to recombination hotspots by PRDM9 and is essential for meiotic double strand break repair. In eLife, 9, . doi:10.7554/eLife.53392. https://pubmed.ncbi.nlm.nih.gov/32744506/
2. Huang, Tao, Yuan, Shenli, Gao, Lei, Chen, Zi-Jiang, Liu, Hongbin. 2020. The histone modification reader ZCWPW1 links histone methylation to PRDM9-induced double-strand break repair. In eLife, 9, . doi:10.7554/eLife.53459. https://pubmed.ncbi.nlm.nih.gov/32374261/
3. Holstege, Henne, Hulsman, Marc, Charbonnier, Camille, Bellenguez, Céline, Lambert, Jean-Charles. 2022. Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. In Nature genetics, 54, 1786-1794. doi:10.1038/s41588-022-01208-7. https://pubmed.ncbi.nlm.nih.gov/36411364/
4. Li, Miao, Huang, Tao, Li, Meng-Jing, Liu, Hong-Bin, Liu, Kui. 2019. The histone modification reader ZCWPW1 is required for meiosis prophase I in male but not in female mice. In Science advances, 5, eaax1101. doi:10.1126/sciadv.aax1101. https://pubmed.ncbi.nlm.nih.gov/31453335/
5. Yuan, Shenli, Huang, Tao, Bao, Ziyou, Liu, Hongbin, Chen, Zi-Jiang. 2022. The histone modification reader ZCWPW1 promotes double-strand break repair by regulating cross-talk of histone modifications and chromatin accessibility at meiotic hotspots. In Genome biology, 23, 187. doi:10.1186/s13059-022-02758-z. https://pubmed.ncbi.nlm.nih.gov/36068616/
6. Song, Yuelin, Guo, Juncen, Zhou, Yanling, Zhang, Guohui, Wang, Hongjing. 2024. A loss-of-function variant in ZCWPW1 causes human male infertility with sperm head defect and high DNA fragmentation. In Reproductive health, 21, 18. doi:10.1186/s12978-024-01746-9. https://pubmed.ncbi.nlm.nih.gov/38310235/
7. Mahgoub, Mohamed, Paiano, Jacob, Bruno, Melania, Nussenzweig, André, Macfarlan, Todd S. 2020. Dual histone methyl reader ZCWPW1 facilitates repair of meiotic double strand breaks in male mice. In eLife, 9, . doi:10.7554/eLife.53360. https://pubmed.ncbi.nlm.nih.gov/32352380/
Quality Control Standard
Sperm Test

Pre-cryopreservation: Measurement of sperm concentration, determination of sperm viability.

Post-cryopreservation: A vial of cryopreserved sperms is selected for in-vitro fertilization from each batch.

Environmental Standards:SPF
Available Region:Global
Source:Cyagen
Model Library
Model Library
Resources
Resources
Animal Quality
Animal Quality
Get Support
Get Support
Address:
2255 Martin Avenue, Suite E Santa Clara, CA 95050-2709, US
Tel:
800-921-8930 (8-6pm PST)
+1408-963-0306 (lnt’l)
Fax:
408-969-0338
Email:
animal-service@cyagen.com
service@cyagen.us
CRO Services
OncologyOphthalmologyNeuroscienceMetabolic & CardiovascularAutoimmune & InflammatoryGene TherapyAntibody Therapy
About Us
Corporate OverviewOur PartnersCareersContact Us
Social Media
Disclaimer: Pricing and availability of our products and services vary by region. Listed prices are applicable to the specific countries. Please contact us for more information.
Copyright © 2025 Cyagen. All rights reserved.
Privacy Policy
Site Map
Stay Updated with the Latest from Cyagen
Get the latest news on our research models, CRO services, scientific resources, and special offers—tailored to your research needs and delivered straight to your inbox.
Full Name
Email
Organization
Country
Areas of Interest