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Aia1NZC/Omr
QTL Variant Detail
Summary
QTL variant: Aia1NZC/Omr
Name: autoimmune hemolytic anemia 1; NZC/Omr
MGI ID: MGI:3620161
QTL: Aia1  Location: unknown  Genetic Position: Chr4, Syntenic
Variant
origin
Strain of Specimen:  NZC/Omr
Variant
description
Allele Type:    QTL
Inheritance:    Recessive
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:6517

A locus associated with autoimmune hemolytic anemia was mapped to mouse Chromosome 4 using 100 (NZB/Omr x NZC/Omr)F1 x NZB/Omr and 180 (NZB/Omr x NZC/Omr)F1 x NZC/Omr backcross animals. Parental strain NZB/Omr is highly susceptible (nearly 100% incidence) to spontaneous autoimmune hemolytic anemia compared to parental strain NZC/Omr (0% incidence). Aia1 (autoimmune hemolytic anemia 1) is approximately 36 cM away from Tryp1 (previously known as the coat color gene b), and thought to be located near the minor histocompatibility locus H18 (74.5 cM), a potential candidate gene. Susceptibility to hemolytic autoimmune anemia is derived from the NZB/Omr allele at Aia1. A second unmapped locus, Aia2, is thought to exist. Aia1 and Aia2 are thought to exhibit a dominant or co-dominant effect.

References
Original:  J:6517 Knight JG, et al., Genes determining autoimmune disease in New Zealand mice. J Clin Lab Immunol. 1981 May;5(3):165-70
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
10/22/2024
MGI 6.24
The Jackson Laboratory