Phenotypes Associated with This Genotype

Genotype
MGI:4947127

• Allelic Composition: Calb2^{tm2.1(cre/ERT2)Zjh}/Calb2^{tm2.1(cre/ERT2)Zjh}
• Genetic Background: involves: C57BL/6 * SJL

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

behavior/neurological

impaired coordination ( J:151755 )

• homozygotes are expected to show defects similar to those in mice with null mutations in Calb2, such as impaired motor coordination

nervous system

abnormal nervous system electrophysiology ( J:151755 )

• homozygotes are expected to show defects similar to those in mice with null mutations in Calb2

reduced long-term potentiation ( J:151755 )

• homozygotes are expected to show defects similar to those in mice with null mutations in Calb2, including impaired induction of LTP in the dentate gyrus