Phenotypes Associated with This Genotype

Genotype
MGI:2177316

• Allelic Composition: Tmc1^Mhdabth/Tmc1⁺
• Genetic Background: C3HeB/FeJ-Tmc1^Mhdabth/Ieg

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

behavior/neurological

abnormal gait ( J:86685 )

• characterized as unsteady

hearing/vestibular/ear

deafness ( J:86685 )

• mice lose ability to hear with four to six weeks

• adult mice are completely deaf

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
autosomal dominant nonsyndromic deafness 36		DOID:0110563	OMIM:606705	J:86685
autosomal recessive nonsyndromic deafness 7		DOID:0110520	OMIM:600974	J:86685