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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Mctp1dwnd
deaf wanderer
MGI:6192114
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Mctp1dwnd/Mctp1dwnd B6.B10Sn-Mctp1dwnd/Kjn MGI:6197507
cx2
Mctp1dwnd/Nr2f1tm1.1(KOMP)Mbp involves: C57BL/6J * C57BL/6NJ * C57BL/10SnJ MGI:6197582


Genotype
MGI:6197507
hm1
Allelic
Composition
Mctp1dwnd/Mctp1dwnd
Genetic
Background
B6.B10Sn-Mctp1dwnd/Kjn
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mctp1dwnd mutation (1 available); any Mctp1 mutation (58 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• homozygotes have a moderate circling phenotype, but penetrance is only approximately 35% so this is not a reliable phenotypic determinant.

mortality/aging
N
• Homozygotes do not display postnatal lethality

nervous system
• additional, disorganized inner hair cells are found near the chochlear base, and the density of inner hair cells near the apex and base of the cochlea is greater than in controls, but the cochlea is shorter than normal so the total hair cell number may not be abnormal
• homozygotes have an extra row of outer hair cells at the cochlear apex, although the cochlea is shorter than normal so the total number of hair cells may not be abnormal

hearing/vestibular/ear
• the cochlea is smaller and shorter than that of controls
• shorter than normal
• additional, disorganized inner hair cells are found near the chochlear base, and the density of inner hair cells near the apex and base of the cochlea is greater than in controls, but the cochlea is shorter than normal so the total hair cell number may not be abnormal
• homozygotes have an extra row of outer hair cells at the cochlear apex, although the cochlea is shorter than normal so the total number of hair cells may not be abnormal
• saccule is smaller than normal and not fully separated from the utricle
• duct connecting the saccule and cochlea is larger than normal
• the saccule does not fully separate from the utricle
• the saccule is smaller than normal
• all homozygotes have hearing impairment, with ABR thresholds 20-30 dB higher than controls at one month of age and 25-45 dB higher than controls at six months of age




Genotype
MGI:6197582
cx2
Allelic
Composition
Mctp1dwnd/Nr2f1tm1.1(KOMP)Mbp
Genetic
Background
involves: C57BL/6J * C57BL/6NJ * C57BL/10SnJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Mctp1dwnd mutation (1 available); any Mctp1 mutation (58 available)
Nr2f1tm1.1(KOMP)Mbp mutation (1 available); any Nr2f1 mutation (24 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
hearing/vestibular/ear
• basal cochlea has disorganized hair cells and an excess of inner hair cells, and the apex has extra rows of outer hair cells
• the utricular macula is reduced from an ovate to a trapezoid shape
• the saccular macula is often attached to the utricular macula and cochlear base
• the utricle and saccule fail to properly separate
• transheterozygotes have ABR thresholds 25-50 dB higher than controls at 1 month of age

nervous system
• basal cochlea has disorganized hair cells and an excess of inner hair cells, and the apex has extra rows of outer hair cells





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last database update
09/03/2024
MGI 6.24
The Jackson Laboratory