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Cib2em1Xuzg
Endonuclease-mediated Allele Detail
Summary
Symbol: Cib2em1Xuzg
Name: calcium and integrin binding family member 2; endonuclease-mediated mutation 2, Zhigang Xu
MGI ID: MGI:7612327
Gene: Cib2  Location: Chr9:54452078-54467502 bp, - strand  Genetic Position: Chr9, 29.7 cM
Alliance: Cib2em1Xuzg page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/cas9-mediated recombination using guide RNAs created two deletions of 9 bp and 8 bp in exon 4 resulting in a premature stop codon. RT-PCR confirmed the absence of full length transcript and very low levels of a truncated transcript. (J:280151)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structure(s)
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:280151 Wang Y, et al., Loss of CIB2 Causes Profound Hearing Loss and Abolishes Mechanoelectrical Transduction in Mice. Front Mol Neurosci. 2017;10:401
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
04/16/2024
MGI 6.23
The Jackson Laboratory