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Eae20SJL/J
QTL Variant Detail
Summary
QTL variant: Eae20SJL/J
Name: experimental allergic encephalomyelitis susceptibility 20; SJL/J
MGI ID: MGI:2155282
QTL: Eae20  Location: Chr3:28630453-28630591 bp  Genetic Position: Chr3, cM position of peak correlated region/allele: 12.19 cM
QTL Note: genome coordinates based on the marker associated with the peak LOD score
Variant
origin
Strain of Specimen:  SJL/J
Variant
description
Allele Type:    QTL
Mutation:    Undefined
    This allele confers increased demyelination severity compared to C57BL/10. (J:67840)
Inheritance:    Not Specified
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Notes

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

J:67840

Composite interval mapping (CIM) was performed to identify QTL's involved in experimental allergic encephalomyelitis (EAE), the principal animal model for multiple sclerosis (MS). 173 microsatellite markers were typed in 673 animals from a (B10.S/DvTe x SJL/J)F2 intercross. The SJL/J strain is susceptible to EAE whereas B10S.DvTe is resistant. The authors report 9 novel QTLs in this study, some of which appear to be sex-influenced. Eae15, which affects brain lesion severity, maps to Chromosome 10 from 4 - 19 cM with a LRT (Likelihood Ratio Test Statistic) score of 26.26 in linkage with D10Mit2. Eae16, influencing brain lesion severity (LRT = 19.74) and mononuclear infiltration (LRT = 27.27), maps to Chromosome 12 from 3 - 29 cM in linkage with D12Mit12. Eae20, influencing demyelination (LRT = 17.21), maps to Chromosome 3 from 4 - 23 cM in linkage with D3Mit55. Eae21 and Eae22, QTLs influencing lesion severity (LRT = 25.71 for Eae21; 20.21 for Eae22) and mononuclear infiltration (LRT = 25.90 for Eae21; 16.64 for Eae22) in female mice, mapped to Chromosome 2 from 30 cM - 69 cM in linkage with D2Mit9, and Chromosome 11 from 49 cM - 71 cM in linkage with D11Mit330, respectively. Eae23, influencing lesion severity (LRT = 21.05) and mononuclear infiltration (LRT = 18.95) in male mice, maps to Chromosome 11 from 32 cM - 44 cM in linkage with D11Mit155 and D11Mit194. Eae16 and Eae19, QTLs influencing demyelination (LRT = 17.92 for Eae16; 19.31 for Eae19) in male mice, mapped to Chromosome 12 from 3 cM - 29 cM inlinkage with D12Mit12, and Chromosome 19 from 26 cM - 50 cM in linkage with D19Mit05, respectively. The SJL/J allele increases severity of phenotypes (brain lesion, mononuclear infiltration, and demyelination) at all QTLs discussed in this study.

References
Original:  J:67840 Butterfield RJ, et al., Identification of genetic loci controlling the characteristics and severity of brain and spinal cord lesions in experimental allergic encephalomyelitis. Am J Pathol. 2000 Aug;157(2):637-45
All:  1 reference(s)

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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
11/12/2024
MGI 6.24
The Jackson Laboratory