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Phenotypes Associated with This Genotype
Genotype
MGI:5898375
Allelic
Composition
Cdh23ahl/Cdh23tm1.1Kjn
MahlC57BL/6J/Mahl129S1/SvImJ
Genetic
Background
(129S1.B6-(rs3696307-rs257098870)/Kjn x 129S/Sv-Cdh23tm1.1Kjn/Kjn)F1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cdh23ahl mutation (51 available); any Cdh23 mutation (274 available)
Cdh23tm1.1Kjn mutation (1 available); any Cdh23 mutation (274 available)
Mahl129S1/SvImJ mutation (1 available); any Mahl mutation (2 available)
MahlC57BL/6J mutation (1 available); any Mahl mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• these mice, homozygous for the c.735A point mutation that causes age related hearing loss and heterozgyous for the ameliorating C57BL/6J-derived modifier, have a 16 kHz ABR threshold at 3 months of age that is less than mice homozygous for the 129S1/SvImJ-derived modifier, proving the C57BL/6J allele dominant


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
03/18/2025
MGI 6.24
The Jackson Laboratory