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| Nomenclature |
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Symbol:
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Chd7Ome
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Name:
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chromodomain helicase DNA binding protein 7;
Otitis media and eye defects
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MGI ID: |
MGI:4999643 |
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Gene:
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Chd7
Location:
Chr4:8690406-8867659 bp, + strand
Genetic Position: Chr4,
3.68 cM
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Mutation
origin |
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Strain of Origin:
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BALB/cByJ
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Mutation
description |
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Allele
Type: | |
Spontaneous |
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Mutation: | |
Intragenic deletion |
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Spontaneous mutation deleted exons 2 and 3. (J:187200)
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Inheritance: | |
Dominant |
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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 Chd7 Mutation:
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38 strains or lines available |
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| References |
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Original: |
J:187200
Tian C et al.,
"Otitis media in a new mouse model for CHARGE syndrome with a deletion in the Chd7 gene."
PLoS One 2012;7(4):e34944
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All: |
1 reference(s)
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Analysis Tools
