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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cochtm1Mrtn
targeted mutation 1, Cynthia C Morton
MGI:3814536
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cochtm1Mrtn/Cochtm1Mrtn CBACa.129S4-Cochtm1Mrtn MGI:3814540
ht2
Cochtm1Mrtn/Coch+ CBACa.129S4-Cochtm1Mrtn MGI:4880748


Genotype
MGI:3814540
hm1
Allelic
Composition
Cochtm1Mrtn/Cochtm1Mrtn
Genetic
Background
CBACa.129S4-Cochtm1Mrtn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cochtm1Mrtn mutation (1 available); any Coch mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• ABR thresholds are substantially higher than for wild-types at 21 months of age (J:140594)
• 6 of 8 mice at 21 months of age have no detectable ABR at the maximum stimulus levels of 32 and 41 kHz frequencies (J:140594)
• 4 of 8 mice have no detectable ABR at all frequencies tested (J:140594)
• increase in the ABR threshold can be detected at 19 months of age (J:167669)
• 21 months of age, DPOAEs are substantially smaller (up to 30 dB)
• mice at 19 months have slightly reduced DPOAE for the mid-frequencies (5-10 dB smaller)
• 6 of 8 mice at 21 months of age have no detectable DPOAE at the maximum stimulus levels of 32 and 41 kHz frequencies
• VsEP thresholds are elevated in mice spanning in age from 11 to 21 months (J:140594)
• these thresholds get higher with age (J:140594)
• at 19 and 21 months of age, 2 of 3 mice have no detectable VsEP (J:140594)
• increase in VsEP thresholds at 7 months of age but not at 5 months of age (J:167669)

Mouse Models of Human Disease
DO ID OMIM ID(s) Ref(s)
autosomal dominant nonsyndromic deafness 9 DOID:0110593 OMIM:601369
J:140594 , J:167669




Genotype
MGI:4880748
ht2
Allelic
Composition
Cochtm1Mrtn/Coch+
Genetic
Background
CBACa.129S4-Cochtm1Mrtn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cochtm1Mrtn mutation (1 available); any Coch mutation (43 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• increase in ABR threshold is similar to homozygous mutant mice





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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
12/10/2024
MGI 6.24
The Jackson Laboratory