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| Nomenclature |
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Symbol:
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Cdh23v-ngt
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Name:
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cadherin 23 (otocadherin);
waltzer Niigata
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MGI ID: |
MGI:2154549 |
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Gene:
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Cdh23
Location:
Chr10:60302748-60696490 bp, - strand
Genetic Position: Chr10,
30.11 cM
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Mutation
origin |
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Intragenic deletion |
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Mutation details: A single G nucleotide deletion at codon 49 is predicted to cause a frameshift and premature termination of the encoded protein. (J:69028)
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Inheritance: | |
Recessive |
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Cdh23 Mutation:
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58 strains or lines available |
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| References |
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Original: |
J:69028
Wada T et al.,
"A point mutation in a cadherin gene, Cdh23, causes deafness in a novel mutant, Waltzer mouse niigata."
Biochem Biophys Res Commun 2001 Apr 27;283(1):113-7
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All: |
2 reference(s)
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Analysis Tools
