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Albq13SWR/J
QTL Variant Detail
Summary
QTL variant: Albq13SWR/J
Name: albuminuria QTL 13; SWR/J
MGI ID: MGI:5641734
QTL: Albq13  Location: unknown  Genetic Position: Chr6, Syntenic
Variant
origin
Strain of Specimen:  SWR/J
Variant
description
Allele Type:    QTL
Inheritance:    Not Specified
Notes

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

J:188618

QTL Reference Notes

The Collaborative Cross (CC) is a large (~1,000 line) panel of recombinant inbred (RI) mouse strains being developed through a community effort (Churchill et al. 2004). The CC combines the genomes of eight genetically diverse founder strains - A/J, C57BL/6J, 129S1/SvImJ, NOD/ShiLtJ, NZO/HlLtJ, CAST/EiJ, PWK/PhJ, and WSB/EiJ - to capture nearly 90% of the known variation present in laboratory mice. CC strains are derived using a unique funnel breeding scheme. Once inbred, the RI CC lines can be used to generate thousands of potential 'outbred' but completely reproducible genomes through the generation of recombinant inbred crosses (RIX). The designation 'PreCC' is used to describe a mapping population of CC mice that is still at insipient stages of inbreeding. CTC (2004), Churchill, G. A., et al.. The Collaborative Cross, a community resource for the genetic analysis of complex traits. Nat Genet. 36, 1133-7.

Linkage analysis was performed on 328 (BTBR-T+tf/J x SWR/J)F2 intercross mice using 93 markers to identify QTL associated with albuminuria. Parental strain SWR/J exhibits higher incidence of albuminuria when compared to BTBR-T+tf/J.

QTL Albq13 maps to 6.8 - 32.0 Mb on Chromosome 6 with a peak LOD score of 3.82 at 6.8 cM in linkage with albuminuria. SWR/J alleles confer increased susceptibility to albuminuria.

References
Original:  J:188618 Thaisz J, et al., Genetic analysis of albuminuria in collaborative cross and multiple mouse intercross populations. Am J Physiol Renal Physiol. 2012 Oct;303(7):F972-81
All:  1 reference(s)

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last database update
04/09/2024
MGI 6.23
The Jackson Laboratory