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TauphBALB/cByJ
QTL Variant Detail
Summary
QTL variant: TauphBALB/cByJ
Name: tau phosphorylation; BALB/cByJ
MGI ID: MGI:2664870
QTL: Tauph  Location: Chr16:86076132-86076354 bp  Genetic Position: Chr16, cM position of peak correlated region/allele: 48.89 cM
QTL Note: genome coordinates based on the marker associated with the peak LOD score
Variant
origin
Strain of Specimen:  BALB/cByJ
Variant
description
Allele Type:    QTL
Mutation:    Undefined
    This allele confers increased tau phosphorylation compared to C57BL/6J. (J:81203)
Inheritance:    Dominant
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:81203

Genome scan was performed on a population of (BALB/cByJ-Dab1tm2Cpr x C57BL/6J)F2 animals to identify QTLs associated with tau phosphorylation. The Dab1tm2Cpr mutation is viable on a BALB/cByJ background but not on a 129/Sv x C57BL/6J mixed background. A significant QTL associated with tau phosphorylation, Tauph, mapped to 60 cM on mouse Chromosome 16 with a LOD score of 3.2 at D16Mit224. BALB/cByJ-derived alleles confer increased tau phosphorlyation in a dominant manner at this locus. Possible candidate genes near Tauph are Sod1 and App. Suggestive QTLs mapped to mouse Chromosomes 1 (D1Mit365), 12 (D12Mit014), and 17 (D17Mit142).

References
Original:  J:81203 Brich J, et al., Genetic modulation of tau phosphorylation in the mouse. J Neurosci. 2003 Jan 1;23(1):187-92
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
06/12/2024
MGI 6.13
The Jackson Laboratory