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Phenotypes Associated with This Genotype
Genotype
MGI:3838021
Allelic
Composition
Calytm1.1Cber/Calytm1.1Cber
Genetic
Background
C57BL/6-Calytm1.1Cber
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Calytm1.1Cber mutation (1 available); any Caly mutation (10 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• cultured neurons have defects in clathrin-mediated endocytosis (CME) (J:146583)
• 60 minutes after induction of CME, mutant neurons have two-fold less uptake of tranferrin receptor from the cell surface than controls (J:146583)
• neurons exhibit alterations in stimulated removal of cell surface AMPARs (J:145984)
• GluR1 and GluR2 removal from the cell surface after stimulation with N-methyl-D-aspartate (NMDA) is significantly slower with only 10% removed after 15 minutes of incumbation compared to 50% in wild-type (J:145984)
• treatment of hippocampal neuron cultures with NMDA does not produce a prolonged depression in mEPSC amplitude as it does in wild-type neurons
• using hippocampal CA1 slices, the 58 2% decrease in excitatory post synaptic current detected in WT slices after low frequency stimulation does not occur in mutant CA1 slices


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
06/16/2026
MGI 6.24
The Jackson Laboratory