Cib2em2Mll
Endonuclease-mediated Allele Detail
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| 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
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| Alliance: |
Cib2em2Mll page
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| Allele Type: |
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Endonuclease-mediated (Null/knockout) |
| Mutation: |
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Single point mutation
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Mutation details: Isoleucine 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)
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| 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
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| Carrying any Cib2 Mutation: |
15 strains or lines available
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| 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) |
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