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Phenotypes Associated with This Genotype
Genotype
MGI:3693372
Allelic
Composition
Fyntm1Sor/Fyntm1Sor
Tg(Camk2a-Fyn)1Kndl/0
Genetic
Background
involves: 129S7/SvEvBrd * C57BL/6 * CBA
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Fyntm1Sor mutation (3 available); any Fyn mutation (37 available)
Tg(Camk2a-Fyn)1Kndl mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
nervous system
• do not exhibit rescue of the morphological defects of the hippocampus that are seen in single Fyn homozygotes, however Schaffer collateral LTP is restored
• dorsal part of the dentate gyrus granular cell layer is occasionally perturbed
• caudal part of CA3 pyramidal cell layer is undulated and CA1 pyramidal cells are less tightly packed
• dendritic regions of pyramidal cells are narrow and length of the apical dendrites is shortened
• ectopic pyramidal cells are frequently seen


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
04/16/2024
MGI 6.23
The Jackson Laboratory