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Aod1C57BL/6J
QTL Variant Detail
Summary
QTL variant: Aod1C57BL/6J
Name: autoimmune ovarian dysgenesis 1; C57BL/6J
MGI ID: MGI:2429552
QTL: Aod1  Location: Chr16:32130840-32523112 bp  Genetic Position: Chr16, cM position of peak correlated region/allele: 22.55 cM
QTL Note: genome coordinates based on the boundaries of the QTL region
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:25722

D3Tx, A/J and (D3Tx x A/J)F1 mice are susceptible to AOD (autoimmunne ovarian dysgenesis disease) whereas C57BL/6J mice are resistant thus allowing for the potenial to genetically map the disease within these strains. One hundred and forty-four D3Tx x (C57BL/6J x A/J)F1 x C57BL/6J backcross mice were generated. Based on chi square analysis significant linkage of AOD (gene symbol Aod1) with Chromsome 16 markers D16Mit58 (p = 0.00086) and D16Mit60 (p = 0.00086) was indicated. AOD is distinguished by 2 phenotypes, presence of anti-ovarian antibodies and oophoritis, which when analyzed independently also segregated with markers on Chromsome 16.

References
Original:  J:25722 Wardell BB, et al., Aod1, the immunoregulatory locus controlling abrogation of tolerance in neonatal thymectomy-induced autoimmune ovarian dysgenesis, maps to mouse chromosome 16. Proc Natl Acad Sci U S A. 1995 May 23;92(11):4758-62
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
04/16/2024
MGI 6.23
The Jackson Laboratory