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Tlf2NOD/Smrf
QTL Variant Detail
Summary
QTL variant: Tlf2NOD/Smrf
Name: T lymphocyte fraction 2; NOD/Smrf
MGI ID: MGI:2157569
QTL: Tlf2  Location: unknown  Genetic Position: Chr9, cM position of peak correlated region/allele: 27.07 cM
QTL Note: genome coordinates based on the marker associated with the peak LOD score
Variant
origin
Strain of Specimen:  NOD/Smrf
Variant
description
Allele Type:    QTL
Mutation:    Undefined
    This allele confers increased CD8+ levels in female animals compared to NOD/Lt. (J:49676)
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:49676

The author refines the mapping of a region which governs the unusually high fraction of circulating T lymphocytes in the nonobese diabetic (NOD) mice. Linkage analysis of (NON/Lt x NOD/Smrf)F1 x NOD/Smrf, and (NOD/Smrf x NON/Lt)F1 x NOD/Smrf progeny, and F2 animals from F1 crosses indicates that the phenotype is associated with two regions of mouse Chromosme 9. One region, Tlf, was placed between D9Mit66 (15 cM) and D9Mit2 (17 cM). The second region, Tlf2, was placed distal near D9Mit71 (29 cM).

References
Original:  J:49676 Pearce RB, Fine-mapping of the mouse T lymphocyte fraction (Tlf) locus on chromosome 9: association with autoimmune diabetes. Autoimmunity. 1998;28(1):31-45
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
04/16/2024
MGI 6.23
The Jackson Laboratory