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Organism Name
Myo7ash1/Myo7ash1
RRID:MGI:2449164 RRID Copied  
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RRID:MGI:2449164
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Organism Information

The record is no longer available at this source.

Proper Citation: RRID:MGI:2449164

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

Species: Mus musculus

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

Phenotype: cochlear hair cell degeneration, abnormal organ of Corti morphology, absent pinna reflex, cochlear ganglion degeneration, cochlear hair cell degeneration, deafness, stria vascularis degeneration, increased fluid intake, abnormal behavior, abnormal ear physiology, vestibular saccular macula degeneration, vestibular ganglion hypoplasia, cochlear ganglion degeneration, cochlear ganglion degeneration, impaired swimming, hyperactivity, increased anxiety-related response, slow postnatal weight gain, deafness, reduced male fertility, circling, jerky movement, hyperactivity, gliosis, cochlear ganglion degeneration, head tossing, increased food intake, deafness, cochlear hair cell degeneration, circling, abnormal organ of Corti morphology, abnormal cochlear OHC efferent innervation pattern, cochlear hair cell degeneration, abnormal cochlear hair cell morphology

Affected Gene: Myo7a

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Data and Source Information

Source: Integrated Animals

Source Database: MGI, Mouse Genome Informatics MGI