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Mdwh
Spontaneous Allele Detail
Summary
Symbol: Mdwh
Name: modifier of dw hearing
MGI ID: MGI:5514269
Gene: Mdwh  Location: unknown  Genetic Position: Chr2, Syntenic
Alliance: Mdwh page
Mutation
origin
Strain of Origin:  CAST/EiJ
Mutation
description
Allele Type:    Spontaneous
Mutation:    Undefined
 
Mutation detailsA locus was identified in a cross between DW/J and CAST/EiJ that modified the hearing defect caused by Pou1f1dw but had no affect on hypothyroidism. The locus is on chromosome 2 between 118 and 138-MB (build 37). (J:177740)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Mdwh Mutation:  0 strains or lines available
References
Original:  J:177740 Fang Q, et al., A modifier gene alleviates hypothyroidism-induced hearing impairment in Pou1f1dw dwarf mice. Genetics. 2011 Oct;189(2):665-73
All:  1 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
04/23/2024
MGI 6.23
The Jackson Laboratory