C57BL/6JCya-Kcng4em1flox/Cya
Common Name:
Kcng4-flox
Product ID:
S-CKO-13273
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
Quantity
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Basic Information
Strain Name
Kcng4-flox
Strain ID
CKOCMP-66733-Kcng4-B6J-VA
Gene Name
Product ID
S-CKO-13273
Gene Alias
4921535I01Rik; KV6.3; KV6.4
Background
C57BL/6JCya
NCBI ID
Modification
Conditional knockout
Chromosome
8
Phenotype
Document
Application
--
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Kcng4em1flox/Cya mice (Catalog S-CKO-13273) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000061828
NCBI RefSeq
NM_025734
Target Region
Exon 3
Size of Effective Region
~3.6 kb
Detailed Document
Overview of Gene Research
Kcng4, also known as Kv6.4, is a silent member of the superfamily of voltage-gated potassium (Kv) channels. It expresses in heterotetramers with members of the KCNB (Kv2) family, and is involved in regulating the electrical activity of cells. This gene is of significance in multiple biological processes and disease-related pathways, and genetic models are valuable for studying its functions [1,2,3].
In a transgenic mouse model with targeted deletion of Kcng4 (Kcng4-/-), male sterility occurs due to disturbed spermiogenesis, manifested as a severe reduction in total sperm-cell count, absence of motile spermatozoa, and abnormal sperm morphology. This indicates Kcng4's role in regulating the late stages of spermatogenesis [4]. In zebrafish, different mutations of kcng4b (a zebrafish ortholog) can affect the activity of the Kv channel and cause ear-development defects, such as failure of kinocilia to extend, formation of ectopic otoliths, or failure of otolith development and reduction of kinocilia [2].
In conclusion, Kcng4 is crucial for normal physiological functions in processes like spermatogenesis and ear development. Studies using gene-knockout mouse models and zebrafish models have revealed its significance in these areas, providing insights into the underlying mechanisms of related diseases such as male infertility and potential ear-development disorders.
References:
1. Lacroix, Gabriel, Bhat, Shreyas, Shafia, Zerghona, Blunck, Rikard. 2024. KCNG4 Genetic Variant Linked to Migraine Prevents Expression of KCNB1. In International journal of molecular sciences, 25, . doi:10.3390/ijms25168960. https://pubmed.ncbi.nlm.nih.gov/39201645/
2. Jędrychowska, Justyna, Vardanyan, Vitya, Wieczor, Milosz, Kuznicki, Jacek, Korzh, Vladimir. 2024. Mutant analysis of Kcng4b reveals how the different functional states of the voltage-gated potassium channel regulate ear development. In Developmental biology, 513, 50-62. doi:10.1016/j.ydbio.2024.03.002. https://pubmed.ncbi.nlm.nih.gov/38492873/
3. Jędrychowska, Justyna, Korzh, Vladimir. 2019. Kv2.1 voltage-gated potassium channels in developmental perspective. In Developmental dynamics : an official publication of the American Association of Anatomists, 248, 1180-1194. doi:10.1002/dvdy.114. https://pubmed.ncbi.nlm.nih.gov/31512327/
4. Regnier, Glenn, Bocksteins, Elke, Marei, Waleed F, Leroy, Jo L M R, Snyders, Dirk J. . Targeted deletion of the Kv6.4 subunit causes male sterility due to disturbed spermiogenesis. In Reproduction, fertility, and development, 29, 1567-1575. doi:10.1071/RD16075. https://pubmed.ncbi.nlm.nih.gov/27677211/
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