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Symbol Name ID |
Eps8l2
EPS8-like 2 MGI:2138828 |
| Darker colors indicate more annotations |
| Human Phenotypes | Hearing impairment |
| Disease(s) Associated with EPS8L2 | |
| autosomal recessive nonsyndromic deafness 106 |
| Mouse Phenotypes | abnormal ear morphology |
abnormal cochlear hair cell morphology |
abnormal cochlear hair cell stereociliary bundle morphology |
decreased inner hair cell stereocilia number |
short cochlear hair cell stereocilia |
abnormal hearing electrophysiology |
abnormal auditory brainstem response |
increased or absent threshold for auditory brainstem response |
abnormal auditory summating potential |
decreased cochlear nerve compound action potential |
abnormal distortion product otoacoustic emission |
impaired hearing |
abnormal vestibular system physiology |
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| Availability | Mouse Genotype | |||||||||||||
| Eps8l2tm1b(EUCOMM)Wtsi/Eps8l2tm1b(EUCOMM)Wtsi | ||||||||||||||
| Eps8l2tm1Wma/Eps8l2tm1Wma | ||||||||||||||
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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