Symbol Name ID |
Triobp
TRIO and F-actin binding protein MGI:1349410 |
* | Aspects of the system are reported to show a normal phenotype. |
Darker colors indicate more annotations |
Human Phenotypes | Severe sensorineural hearing impairment |
Disease(s) Associated with TRIOBP | |
autosomal recessive nonsyndromic deafness 28 |
Mouse Phenotypes | hearing/vestibular/ear phenotype |
abnormal cochlear hair cell development |
abnormal inner hair cell stereociliary bundle morphology |
fused inner hair cell stereocilia |
abnormal outer hair cell stereociliary bundle morphology |
fused outer hair cell stereocilia |
decreased cochlear hair cell stereocilia number |
abnormal cochlear hair cell physiology |
abnormal auditory brainstem response |
increased or absent threshold for auditory brainstem response |
deafness |
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Availability | Mouse Genotype | |||||||||||
Triobpem1(IMPC)J/Triobpem1(IMPC)J | ||||||||||||
Triobptm1Tbf/Triobptm1Tbf | * |
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 04/30/2024 MGI 6.23 |
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