Symbol Name ID |
Eps8
epidermal growth factor receptor pathway substrate 8 MGI:104684 |
Darker colors indicate more annotations |
Human Phenotypes | Profound hearing impairment |
Disease(s) Associated with EPS8 | |
autosomal recessive nonsyndromic deafness 102 |
Mouse Phenotypes | short cochlear hair cell stereocilia |
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Availability | Mouse Genotype | |
Eps8tm1Ppdf/Eps8tm1Ppdf |
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 04/09/2024 MGI 6.23 |
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