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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
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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: 0 strains 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)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory