Phenotypes Associated with This Genotype

Genotype
MGI:5311851

• Allelic Composition: Cep41^{Gt(AW0157)Wtsi}/Cep41^{Gt(AW0157)Wtsi}
• Genetic Background: involves: 129P2/OlaHsd * C57BL/6

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

mortality/aging

embryonic lethality during organogenesis, incomplete penetrance ( J:181179 )

• between E10 to E12

embryo

embryo phenotype ( J:181179 )

N • some embryos show normal development

abnormal embryo turning ( J:181179 )

• rotation failure in some embryos

cardiovascular system

abnormal pericardium morphology ( J:181179 )

• dilated pericardial sac in some embryos

intracranial hemorrhage ( J:181179 )

• brain hemorrhage in some embryos

nervous system

intracranial hemorrhage ( J:181179 )

• brain hemorrhage in some embryos

abnormal hindbrain morphology ( J:181179 )

• mild malformation in some embryos

exencephaly ( J:181179 )

• in some embryos