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Mpdk8C57BL/6J
QTL Variant Detail
Nomenclature
QTL variant: Mpdk8C57BL/6J
Name: modifier of polycystic kidney disease 8; C57BL/6J
MGI ID: MGI:3603247
QTL: Mpdk8  Location: unknown  Genetic Position: Chr3, Syntenic
Variant
origin
Strain of Specimen:  C57BL/6J
Variant
description
Allele Type:    QTL
Inheritance:    Other (see notes)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 anatomical structures
Notes
Mpdk8 exhibits additive inheritance.

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

J:99468

Linkage analysis was performed on 461 homozygous mutant animals from a (C57BL/6J-Cys1cpk x CAST/Ei)F2 intercross to identify modifiers of the Cys1cpk mutation. 79 microsatellite markers at an average spacing of 25 cM were used in the genome scan. C57BL/6J-Cys1cpk mutant animals exhibit cystic kidney disease and biliary dysgenesis.

Major modifier loci mapped to 16 cM, 34 cM, and 54 cM on mouse Chromosome 4 in linkage to renal traits and biliary ductal expansion. These loci are named Mpdk1 (modifierof polycystic kidney disease 1), Mpdk2, and Mpdk3, respectively. Mpdk3 also shows linkage to cholangitis (LOD=4.8). CAST/Ei-derived alleles at Mpdk1, Mpdk2, and Mpdk3 confer increased renal traits (kidney length, weight, and volume) with a dominant mode of inheritance. Kif12 maps to the Mpdk2 region and is proposed as a candidate gene. The C57BL/6J allele of Kif12 has a 15 bp deletion corresponding to a 5 amino acid deletion in the predicted L2 loop of the kinesin molecular motor catalytic domain. In addition, the CAST/Ei Kif12 haplotype shows strong correlation with polycystic kidney disease severity in (C57BL/6J-Cys1cpk x CAST/Ei)F2 mice.

Linkage to renal traits mapped to 26 cM on mouse Chromosome 1 with LOD=2.5. This locus is named Mpdk4 (modifier of polycystic kidney disease 4). CAST/Ei-derived alleles at Mpdk4 confer increased renal traits with an additive mode of inheritance.

Linkage to renal traits mapped to 8 cM on mouse Chromosome 2 with LOD=3.2. This locus is named Mpdk5 (modifier of polycystic kidney disease 5). CAST/Ei-derived alleles at Mpdk5 confer increased renal traits with an additive mode of inheritance.

Linkage to biliary ductal expansion mapped to 16 cM on mouse Chromosome 13 with LOD=6.8. This locus is named Mpdk6 (modifier ofpolycystic kidney disease 6) and exhibits overdominance.

Linkage to cholangitis mapped to 40 cM on mouse Chromosome 19 with LOD=2.7. This locus is named Mpdk7 (modifier of polycystic kidney disease 7). CAST/Ei-derived alleles at Mpdk7 confer increased cholangitis with an additive mode of inheritance.

Linkage to cholangitis mapped to 6 cM on mouse Chromosome 3 with LOD=3.3. This locus is named Mpdk8 (modifier of polycystic kidney disease 8). CAST/Ei-derived alleles at Mpdk8 confer increased cholangitiswith an additive mode of inheritance.

Interaction between loci at 62 cM on mouse Chromosome 1 and 96 cM on mouse Chromosome 2 was detected for effects on biliary duct expansion. A second interacting locus pair affecting biliary duct expansion was detected between 14 cM on mouse Chromosome 4 and 17 cM on mouse Chromosome 18.

References
Original:  J:99468 Mrug M, et al., Kinesin family member 12 is a candidate polycystic kidney disease modifier in the cpk mouse. J Am Soc Nephrol. 2005 Apr;16(4):905-16
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
02/23/2021
MGI 6.16
The Jackson Laboratory