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Hcbip2C57BL/10ScSn
QTL Variant Detail
Nomenclature
QTL variant: Hcbip2C57BL/10ScSn
Name: hexachlorobenzene induced porphyria 2; C57BL/10ScSn
MGI ID: MGI:2429734
QTL: Hcbip2  Location: Chr17:37793055-45622654 bp  Genetic Position: Chr17, Syntenic
Variant
origin
Strain of Specimen:  C57BL/10ScSn
Variant
description
Allele Type:    QTL
Notes

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

J:52511

Human porphyrias can be modelled in iron-loaded mice exposed to hexachlorobenzene. C57BL/10ScSn is a protoytpe susceptible strain whereas DBA/2 mice are extremely resistant. A search for susceptibility loci was undertaken using QTL analysis with microsatellite markers of high and low responders from an F2 intercross. Susceptibility is defined as the accumulation of uroporphrin in the liver. Statistical analysis revealed the presence of a region on mouse Chromosome 17 between D17Mit49 and D17Mit24 associated with porphyria susceptibility (LOD = 3.6). This locus was assigned the symbol Hcbip2.

References
Original:  J:52511 Akhtar RA, et al., Chromosomal linkage analysis of porphyria in mice induced by hexachlorobenzene-iron synergism: a model of sporadic porphyria cutanea tarda. Pharmacogenetics. 1998 Dec;8(6):485-94
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
08/03/2022
MGI 6.21
The Jackson Laboratory