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| Caption | Cochlear dysgenesis caused by loss of Fgf20 in the developing cochlear sensory epithelium. (B) Histology of the inner ear showing normal organ of Corti structure in wild-type and Fgf20tm1.1Dor/Fgf20+ cochlea in which there are three outer hair cells (OHC), one inner hair cell (IHC), three Deiters' cells (DC), two pillar cells (PC), and several inner phalangeal cells (IPhC). Fgf20tm1.1Dor/Fgf20tm1.1Dor cochlea showed disorganization and loss of sensory cells in the organ of Corti. Scale bar: 100 um. | ||||
| Copyright | This image is from Huh SH, PLoS Biol 2012 Jan;10(1):e1001231, and is displayed under the terms of the Creative Commons Attribution 4.0 International License. J:184501 | ||||
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Associated Genotypes |
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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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