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Mcal3B6.129P2-Apoe-tm1Unc/J
QTL Variant Detail
Summary
QTL variant: Mcal3B6.129P2-Apoe-tm1Unc/J
Name: medial calcification 3; B6.129P2-Apoetm1Unc/J
MGI ID: MGI:5697496
QTL: Mcal3  Location: unknown  Genetic Position: Chr18, Syntenic
Variant
origin
Strain of Specimen:  B6.129P2-Apoetm1Unc/J
Variant
description
Allele Type:    QTL
Inheritance:    Not Specified
Notes
Mcal3 is male-specific.

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

J:182797

Linkage analysis was performed on 332 (B6.129P2-Apoetm1Unc/J x C3.129P2(B6)-Apoetm1Unc)F2 intercross mice using 1347 markers to identify QTL associated with aortic medial calcification. Parental strain C3H/HeJ displays higher susceptibility to aortic medial disruption than C57BL/6J.

QTL Mcal3 maps to 7.4 - 77.9 Mb on Chromosome 18 with a peak LOD score of 2.76 (sex-covariate) or 4.79 (sex-interaction) at 43.7 cM in linkage with aortic medial calcification. C57BL/6J alleles confer increased susceptibility to aortic medial calcification at the Mcal3 locus. Mcal3 is a male-specific QTL.

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
04/23/2024
MGI 6.23
The Jackson Laboratory