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Chd7Ome
Spontaneous Allele Detail
Nomenclature
Symbol: Chd7Ome
Name: chromodomain helicase DNA binding protein 7; Otitis media and eye defects
MGI ID: MGI:4999643
Gene: Chd7  Location: Chr4:8690406-8867659 bp, + strand  Genetic Position: Chr4, 3.68 cM
Ear abnormalities in Chd7Ome/Chd7+ mice

Show the 4 phenotype image(s) involving this allele.

Mutation
origin
Strain of Origin:  BALB/cByJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Intragenic deletion
    Spontaneous mutation deleted exons 2 and 3. (J:187200)
Inheritance:    Dominant
Molecular structure of the Chd7Ome mutation
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Disease models
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Expression
In Structures Affected by this Mutation: 7 anatomical structures
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 Chd7 Mutation:  91 strains or lines available
References
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
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/18/2018
MGI 6.12
The Jackson Laboratory