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C57BL/6JCya-Whrnem1/Cya
Common Name:
Whrn-KO
Product ID:
S-KO-14208
Background:
C57BL/6JCya
Product Type
Age
Genotype
Sex
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Basic Information
Strain Name
Whrn-KO
Strain ID
KOCMP-73750-Whrn-B6J-VA
Gene Name
Whrn
Product ID
S-KO-14208
Gene Alias
1110035G07Rik; C430046P22Rik; Dfnb31; Ush2d; wi
Background
C57BL/6JCya
NCBI ID
73750
Modification
Conventional knockout
Chromosome
4
Phenotype
MGI:2682003
Document
Click here to download >>
Application
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Rare Disease Data Center >>
Note
Note: When using this mouse strain in a publication, please cite “C57BL/6JCya-Whrnem1/Cya mice (Catalog S-KO-14208) were purchased from Cyagen.”
Strain Description
Ensembl Number
ENSMUST00000084510
NCBI RefSeq
NM_001008791
Target Region
Exon 4
Size of Effective Region
~2.3 kb
Detailed Document
Click here to download >>
Overview of Gene Research
WHRN, encoding a cytoskeletal scaffold protein, is involved in binding membrane protein complexes to the cytoskeleton in ocular photoreceptors and ear hair cell stereocilia. It is part of the ankle-link complex (ALC) along with USH2A, PDZD7, and ADGRV1, which is crucial for hair cell development [1,2,3]. Mutations in WHRN are associated with non-syndromic hearing loss and Usher syndrome type II [2].

In a study establishing Adgrv1 Y6236fsX1 mutant mice as a model for a deafness-associated human mutation, it was shown that the mutation disrupts the interaction between ADGRV1 and other ALC components, including WHRN. ADGRV1 normally inhibits WHRN phosphorylation through regional cAMP-PKA signaling, which in turn regulates the ubiquitination and stability of USH2A. The mutant ADGRV1 fails to do so, leading to stereocilia disorganization and mechanoelectrical transduction deficits [1]. Also, in a Moroccan family, whole exome sequencing identified a homozygous WHRN gene variant (c.619G > T; p.Ala207Ser) in a patient with severe hearing loss, and bioinformatics methods predicted the pathogenic implications of this variation [2].

In conclusion, WHRN is essential for the proper functioning of the ankle-link complex in hair cell development. Studies using mouse models have revealed its role in maintaining the stability of ALC components and normal stereocilia function, with implications for understanding the pathogenesis of hearing-related diseases such as Usher syndrome and non-syndromic hearing loss [1,2].

References:

1. Guan, Ying, Du, Hai-Bo, Yang, Zhao, Sun, Jin-Peng, Xu, Zhi-Gang. 2023. Deafness-Associated ADGRV1 Mutation Impairs USH2A Stability through Improper Phosphorylation of WHRN and WDSUB1 Recruitment. In Advanced science (Weinheim, Baden-Wurttemberg, Germany), 10, e2205993. doi:10.1002/advs.202205993. https://pubmed.ncbi.nlm.nih.gov/37066759/

2. AitRaise, Imane, Amalou, Ghita, Redouane, Salaheddine, Petit, Christine, Barakat, Abdelhamid. 2023. Novel pathogenic WHRN variant causing hearing loss in a moroccan family. In Molecular biology reports, 50, 10663-10669. doi:10.1007/s11033-023-08901-8. https://pubmed.ncbi.nlm.nih.gov/37924449/

3. Wang, Huang, Du, Haibo, Ren, Rui, Xu, Zhigang, Lu, Qing. 2023. Temporal and spatial assembly of inner ear hair cell ankle link condensate through phase separation. In Nature communications, 14, 1657. doi:10.1038/s41467-023-37267-5. https://pubmed.ncbi.nlm.nih.gov/36964137/

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
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