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Symbol Name ID |
Ercc8
excision repaiross-complementing rodent repair deficiency, complementation group 8 MGI:1919241 |
| Darker colors indicate more annotations |
| Human Phenotypes | Abnormal pinna morphology |
Macrotia |
Sensorineural hearing impairment |
High-frequency sensorineural hearing impairment |
Progressive sensorineural hearing impairment |
Hearing impairment |
| Disease(s) Associated with ERCC8 | ||||||
| Cockayne syndrome | ||||||
| Cockayne syndrome A |
| Mouse Phenotypes | cochlear inner hair cell degeneration |
cochlear outer hair cell degeneration |
increased or absent threshold for auditory brainstem response |
decreased distortion product otoacoustic emission amplitude |
impaired hearing |
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| Availability | Mouse Genotype | |||||
| Ercc8tm1Jhjh/Ercc8tm1Jhjh | ||||||
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 04/16/2024 MGI 6.23 |
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