About   Help   FAQ
Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(Camk2a-Fyn)1Kndl
transgene insertion 1, Eric R Kandel
MGI:2446639
Summary 1 genotype
Jump to Allelic Composition Genetic Background Genotype ID
cx1
Fyntm1Sor/Fyntm1Sor
Tg(Camk2a-Fyn)1Kndl/0
involves: 129S7/SvEvBrd * C57BL/6 * CBA MGI:3693372


Genotype
MGI:3693372
cx1
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 (39 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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory