Phenotypes Associated with This Genotype

Genotype
MGI:7481298

• Allelic Composition: Ccser2^em1Skpk/Ccser2^em1Skpk
• Genetic Background: C57BL/6N-Ccser2^em1Skpk

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

mortality/aging

postnatal lethality, incomplete penetrance ( J:333716 )

• fewer than expected mice are present at P28

• however, normal numbers of mice are present at E18.5

nervous system

abnormal neuronal migration ( J:333716 )

• with a decrease in the length without changing the orientation of the leading process

abnormal cerebral cortex morphology ( J:333716 )

• impaired cortical lamination

cellular

abnormal neuronal migration ( J:333716 )

• with a decrease in the length without changing the orientation of the leading process