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Symbol Name ID |
Nfix
nuclear factor I/X MGI:97311 |
| Darker colors indicate more annotations |
| Human Phenotypes | Cholesteatoma |
Conductive hearing impairment |
Bilateral conductive hearing impairment |
Overfolded helix |
Low-set ears |
Hearing impairment |
| Disease(s) Associated with NFIX | ||||||
| Marshall-Smith syndrome |
| Mouse Phenotypes | abnormal inner ear canal morphology |
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| Availability | Mouse Genotype | |
| Nfixtm1.1Rmg/Nfixtm1.1Rmg | ||
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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