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Lmb2MRL/MpScr
QTL Variant Detail
Summary
QTL variant: Lmb2MRL/MpScr
Name: lupus in MRL and B6 F2 cross, QTL 2; MRL/MpScr
MGI ID: MGI:2156221
QTL: Lmb2  Location: Chr5:37581488-112465722 bp  Genetic Position: Chr5, Syntenic
Variant
origin
Strain of Specimen:  MRL-Faslpr
Variant
description
Allele Type:    QTL
Mutation:    Undefined
 
Mutation detailsThis allele confers susceptibility to splenomegaly, lymphadenopathy, and anti-dsDNA antibody production compared to C57BL/6. (J:45708)
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: 2 anatomical structure(s)
Notes
This allele is consistent with a dominant or additive mode of inheritance.

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

J:45708

In a (MRL-Tnfrsf6lpr x C57BL/6-Tnfrsf6lpr)F1 cross involving 274 F2 progeny a quantitative trait locus, Lmb2, identifying lymphadenopathy and/or splenomegaly was significantly associated with a region of mouse Chromosome 5 flanked by markers D5Mit13 and D5Mit24. The highest LOD scores were associated with D5Mit356.

References
Original:  J:45708 Vidal S, et al., Loci predisposing to autoimmunity in MRL-Fas lpr and C57BL/6-Faslpr mice. J Clin Invest. 1998 Feb 1;101(3):696-702
All:  2 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
10/29/2024
MGI 6.24
The Jackson Laboratory