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Aasm1B6.129P2-Apoe-tm1Unc/J
QTL Variant Detail
Summary
QTL variant: Aasm1B6.129P2-Apoe-tm1Unc/J
Name: aortic aneurysm 1; B6.129P2-Apoetm1Unc/J
MGI ID: MGI:5697463
QTL: Aasm1  Location: unknown  Genetic Position: Chr6, Syntenic
Variant
origin
Strain of Specimen:  B6.129P2-Apoetm1Unc/J
Variant
description
Allele Type:    QTL
Inheritance:    Not Specified
Notes

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

J:182797

Linkage analysis was performed on 332 (B6.129P2-Apoe-tm1Unc/J x C3.129P2(B6)-Apoe-tm1Unc)F2 intercross mice using 1347 markers to identify QTL associated with aortic medial disruption. Parental strain C3H/HeJ displays higher susceptibility to aortic medial disruption than C57BL/6J.

QTL Aasm1 maps to 43.7 - 127.5 Mb on Chromosome 6 with a peak LOD score of 6.81 (sex-covariate) or 5.93 (sex-interaction) at 74 cM in linkage with aortic medial disruption. Because of an inversion in the C3H/HeJ strain on chromosome 6, 74 cM may not accurately reflect the actual peak location of the Aasm1 QTL. C57BL/6J alleles confer decreased susceptibility to aortic medial disruption at the Aasm1 locus.

References
Original:  J:182797 Wang SS, et al., Disruption of the aortic elastic lamina and medial calcification share genetic determinants in mice. Circ Cardiovasc Genet. 2009 Dec;2(6):573-82
All:  1 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
11/12/2024
MGI 6.24
The Jackson Laboratory