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Organism Name
Pou1f1dw/Pou1f1dw
RRID:MGI:3653204 RRID Copied  
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RRID:MGI:3653204
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Organism Information

The record is no longer available at this source.

Proper Citation: RRID:MGI:3653204

Description: Allele Detail: Spontaneous This is a legacy resource.

Species: Mus musculus

Notes: Allele Detail: Spontaneous This is a legacy resource.

Phenotype: decreased prolactin level, decreased growth hormone level, cochlear outer hair cell degeneration, abnormal Hensen stripe morphology, absent distortion product otoacoustic emissions, absent cochlear microphonics, abnormal tunnel of Corti morphology, abnormal tectorial membrane striated-sheet matrix morphology, abnormal pillar cell morphology, abnormal orientation of outer hair cell stereociliary bundles, abnormal hair cell physiology, abnormal cochlear outer hair cell morphology, abnormal actin cytoskeleton morphology, abnormal molar root morphology, proportional dwarf, infertility, abnormal strial intermediate cell morphology, absent somatotrophs, abnormal tectorial membrane morphology, decreased endocochlear potential, short cochlear outer hair cells, deafness, abnormal stria vascularis morphology, absent lactotrophs, decreased circulating prolactin level, decreased thyrotroph cell number

Affected Gene: Pou1f1

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Data and Source Information

Source: Integrated Animals

Source Database: MGI, Mouse Genome Informatics MGI