Jckm1^C57BL/6J
QTL Variant Detail

Summary

• QTL variant: Jckm1^C57BL/6J
• Name: juvenile cystic kidney modifier 1; C57BL/6J
• MGI ID: MGI:5636758
• QTL: Jckm1 Location: Chr10:118497164-120735487 bp Genetic Position: Chr10, cM position of peak correlated region/allele: 34.83 cM
• QTL Note: genome coordinates based on the marker associated with the peak LOD score

Variant origin

• Strain of Specimen: C57BL/6J

Variant description

• Allele Type: QTL

Notes

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

J:23893

Jckm1 was mapped between D10Mit14 and D10Mit102 on mouse Chromosome 10 using 55 F2 progeny from the (C57BL/6J x DBA/2J)F1 jck /+ intercross and quantitative trait locus analysis. The LOD score for placing Jckm1 in the region bewteen D1Mit14 and D10Mit102is 2.0.

J:43909

(C57BL/6J x DBA/2J)F2-jck/+ intercross animals were used to map QTLs that modify the severity of polycystic kidney disease (PKD). The parental C57BL/6J strain used in this cross carries a homozygous mutation in the jck gene resulting in enhanced PKD phenotype (increased kidney weight). DBA/2J is wild type at the jck locus and exhibits a mild PKD phenotype. Jckm1 (juvenile cystic kidney modifier 1) mapped to chromosome 10 with a peak LOD score of 2.1 between D10Mit14 (65 cM) and D10Mit102 (69 cM). DBA/2J-derived alleles at this locus appear to increase PKD severity in an additive fashion. Jckm2 mapped to chromosome 1 with a peak LOD score of 16.8 between D1Mit7 (41 cM) and D1Mit30 (70 cM). C57BL/6J-derived alleles confer recessively inherited susceptibility to PKD at this locus. There appears to be strain-specific interactions between Jckm1 and Jckm2: animals homozygous for C57BL/6J-like alleles at Jckm2 and homozygous for DBA/2J-like alleles at Jckm1 develop severe PKD.

References

• Original: J:23893 Iakoubova OA, et al., Localization of a murine recessive polycystic kidney disease mutation and modifying loci that affect disease severity. Genomics. 1995 Mar 1;26(1):107-14
• All: 2 reference(s)