About   Help   FAQ
Clrn2em1H
Endonuclease-mediated Allele Detail
Summary
Symbol: Clrn2em1H
Name: clarin 2; endonuclease-mediated mutation 1, Harwell
MGI ID: MGI:6458758
Synonyms: Clrn2del629
Gene: Clrn2  Location: Chr5:45611093-45621491 bp, + strand  Genetic Position: Chr5, Syntenic
Alliance: Clrn2em1H page
Mutation
origin
Strain of Origin:  Not Applicable
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
    CRISPR-targeting deleted 629 bp of exon 2. (J:283627)
Phenotypes
Loading...
View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Clrn2 Mutation:  26 strains or lines available
References
Original:  J:283627 Dunbar LA, et al., Clarin-2 is essential for hearing by maintaining stereocilia integrity and function. EMBO Mol Med. 2019 Sep;11(9):e10288
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
10/29/2024
MGI 6.24
The Jackson Laboratory