Phenotypes Associated with This Genotype

Genotype
MGI:3829509

• Allelic Composition: Eif3c^Xs/Eif3c⁺
• Genetic Background: Not Specified

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

mortality/aging

decreased survivor rate ( J:14234 )

• Background Sensitivity: due to reduced penetrance or viability

limbs/digits/tail

abnormal limb morphology ( J:14234 )

• severe limb defects including absence of major bones

abnormal hallux morphology ( J:14234 )

• on the hindfeet occasionally the first digit of one or both feet may be thickened, twisted, or duplicated

polydactyly ( J:14234 )

• develops preaxially on one or both forefeet

• the left forefoot is affected more frequently than the right

pigmentation

white spotting ( J:14234 )

• not typical of all mice

• amount varies from a few white hairs to a defined patch

belly spot ( J:14234 )

• usually on the belly

head spot ( J:14234 )

• not always seen

craniofacial

abnormal outer ear morphology ( J:14234 )

• occasionally the pinna is abnormal

hearing/vestibular/ear

abnormal outer ear morphology ( J:14234 )

• occasionally the pinna is abnormal

integument

white spotting ( J:14234 )

• not typical of all mice

• amount varies from a few white hairs to a defined patch

belly spot ( J:14234 )

• usually on the belly

head spot ( J:14234 )

• not always seen

growth/size/body

abnormal outer ear morphology ( J:14234 )

• occasionally the pinna is abnormal