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Phenotype Image Detail
Image
Caption Morphological defects at the basal turn of the cochlea in the Cldn9nmf329/Cldn9nmf329 mouse line. (A-D) Hematoxylin- and eosin-stained cross sections of cochleas from wild-type (+/+) and mutant mice (P28), at the basal turn (base) and apical turn (apex). In contrast to the intact cochlear morphology of a control mouse (A), the basal cochlear turn of a mutant mouse lacks the tunnel of Corti and contains only two rows of outer hair cells (OHCs) (B). The apical turn of the cochlea is intact in both the wild-type and mutant mice (C, D). Arrows indicate the OHCs in the mutant sample. Scale bars: 100 um.
Copyright This image is from Nakano Y, PLoS Genet 2009 Aug;5(8):e1000610, and is displayed under the terms of the Creative Commons Attribution 4.0 International License. J:152154
Associated
Alleles
Symbol Name
Cldn9nmf329 claudin 9; neuroscience mutagenesis facility, 329
Associated
Genotypes
Allelic Composition Genetic Background
Cldn9nmf329/Cldn9nmf329 C57BL/6J-Cldn9nmf329/J

Contributing Projects:
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
04/23/2024
MGI 6.23
The Jackson Laboratory