Mdwh
Spontaneous Allele Detail
|
|
| Symbol: |
Mdwh |
| Name: |
modifier of dw hearing |
| MGI ID: |
MGI:5514269 |
| Gene: |
Mdwh Location: unknown Genetic Position: Chr2, Syntenic
|
| Alliance: |
Mdwh page
|
|
|
|
| Allele Type: |
|
Spontaneous |
| Mutation: |
|
Undefined
|
| |
|
Mutation details: A 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)
|
|
|
View phenotypes and curated references for all genotypes (concatenated display).
|
| 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
|
|
| 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) |
|
Analysis Tools
