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Asp3DBA/2J
QTL Variant Detail
Summary
QTL variant: Asp3DBA/2J
Name: audiogenic seizure prone 3; DBA/2J
MGI ID: MGI:1856807
QTL: Asp3  Location: Chr7:27305798-36842367 bp  Genetic Position: Chr7, Syntenic
Variant
origin
Strain of Specimen:  DBA/2J
Variant
description
Allele Type:    QTL
Inheritance:    Recessive
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Notes

Mapping and Phenotype information for this QTL, its variants and associated markers

J:1300

Backcross mice from (A/J x DBA/2J)F1 x A/J and (A/J x DBA/1J)F1 x A/J matings were tested for seizure susceptibility. A statistical association of susceptibility of seizures with the albino locus was indicated. The seizure susceptibility locus on Chromosome 7 is Asp3. Mice from reciprocal crosses involving these strains were tested to show that parental imprinting was not a factor in the seizure susceptibility involving Asp3.

J:43137

The asp3 locus was mapped as a quantitative trait between markers D7Mit77 and D7Mit247 in the EP (epilepsy prone) female x (EP x DBA/2J)F1 male backcross. The reciprocal backcross did not show linkage to the mouse Chromosome 7 markers, suggesting that asp3 is influenced by genetic imprinting.

References
Original:  J:11261 Neumann PE, et al., Genetic dissection of susceptibility to audiogenic seizures in inbred mice. Proc Natl Acad Sci U S A. 1991 Jun 15;88(12):5408-12
All:  2 reference(s)

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
12/10/2024
MGI 6.24
The Jackson Laboratory