Phenotypes Associated with This Genotype

Genotype
MGI:3838502

• Allelic Composition: Hmx1^mpe/Hmx1^mpe
• Genetic Background: C3H/HeJ-Hmx1^mpe/J

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

Hmx1^mpe/Hmx1^mpe mouse

mortality/aging

perinatal lethality, incomplete penetrance ( J:147782 )

• heterozygous intercrosses yield fewer than anticipated homozygotes, 36 instead of 46.75 out of 187 pups

craniofacial

abnormal ear position ( J:147782 )

• unusually large or abnormally oriented ear lobes

lowered ear position ( J:147782 )

hearing/vestibular/ear

abnormal ear position ( J:147782 )

• unusually large or abnormally oriented ear lobes

lowered ear position ( J:147782 )

growth/size/body

abnormal ear position ( J:147782 )

• unusually large or abnormally oriented ear lobes

lowered ear position ( J:147782 )

decreased body size ( J:147782 )

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
oculoauricular syndrome		DOID:0060482	OMIM:612109	J:147782