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Cib2em2Mll
Endonuclease-mediated Allele Detail
Summary
Symbol: Cib2em2Mll
Name: calcium and integrin binding family member 2; endonuclease-mediated mutation 2, Ulrich Muller
MGI ID: MGI:7529459
Synonyms: Cib2-I123T, Cib2I123T
Gene: Cib2  Location: Chr9:54452078-54467502 bp, - strand  Genetic Position: Chr9, 29.7 cM
Alliance: Cib2em2Mll page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Single point mutation
 
Mutation detailsIsoleucine codon 123 (ATC) in exon 5 was changed to threonine (ACC) (p.I123T) using crRNA, tracrRNA and an ssODN template with CRISPR/Cas9 technology. The mutation affects mechanoelectrical transduction (MET) by cochlear hair cells and causes deafness. (J:307668)
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 Cib2 Mutation:  15 strains or lines available
References
Original:  J:307668 Liang X, et al., CIB2 and CIB3 are auxiliary subunits of the mechanotransduction channel of hair cells. Neuron. 2021 Jul 7;109(13):2131-2149.e15
All:  1 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
01/06/2026
MGI 6.24
The Jackson Laboratory