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Phenotypes Associated with This Genotype
Genotype
MGI:4441378
Allelic
Composition
Gja1tm1Kwi/Gja1tm1Kwi
Tg(S100b-cre)20Ito/0
Genetic
Background
involves: 129P2/OlaHsd * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Gja1tm1Kwi mutation (1 available); any Gja1 mutation (60 available)
Tg(S100b-cre)20Ito mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
N
• cytoarchitecture of the adult brain appears normal; at 1.5 months, Bergmann glial processes show no morphologic abnormalites and Purkinje cell dendrite branching is normal
• cerebellar LTD induction and maintenance is not affected; no loss of astrocytes in the cerebellar cortex are detected in mutants
• intercellular coupling of Bergmann glial cells (through gap junctions) as indicated by dye injection is significantly reduced compared to Gja1tm1Kwi homozygous controls at 3.5 months

behavior/neurological
N
• no enhanced locomotor activity or increased exploratory behavior is observed in open field tests
• associative motor learning (in delay eyeblink conditioning) is similar between mutants and controls at 3-3.5 months

cellular
• intercellular coupling of Bergmann glial cells (through gap junctions) as indicated by dye injection is significantly reduced compared to Gja1tm1Kwi homozygous controls at 3.5 months


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
03/25/2025
MGI 6.24
The Jackson Laboratory