Phenotypes Associated with This Genotype

Genotype
MGI:5308948

• Allelic Composition: Ctnnb1^tm1Kba/Ctnnb1^tm1Kba
• Genetic Background: involves: 129S6/SvEvTac * C57BL/6

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

craniofacial

abnormal craniofacial development ( J:178971 )

• defects are seen in 43% of embryos at E10.5

small pharyngeal arch ( J:178971 )

• rudimentary at E10.5

embryo

small pharyngeal arch ( J:178971 )

• rudimentary at E10.5

embryonic growth retardation ( J:178971 )

• visible at E10

decreased embryo size ( J:178971 )

• at E10

nervous system

abnormal forebrain development ( J:178971 )

• at E10.5

growth/size/body

embryonic growth retardation ( J:178971 )

• visible at E10

decreased embryo size ( J:178971 )

• at E10