About   Help   FAQ
Hfib1A/J
QTL Variant Detail
Summary
QTL variant: Hfib1A/J
Name: hepatic fibrogenesis 1; A/J
MGI ID: MGI:2661490
QTL: Hfib1  Location: Chr15:64306334-64306479 bp  Genetic Position: Chr15, cM position of peak correlated region/allele: 29.03 cM
QTL Note: genome coordinates based on the marker associated with the peak LOD score
Variant
origin
Strain of Specimen:  A/J
Variant
description
Allele Type:    QTL
Inheritance:    Dominant
Notes

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

J:80619

Linkage analysis was performed on 358 animals from an (A/J x BALB/cJ)F2 cross with an average marker resolution of 20 cM to identify QTLs influencing hepatic fibrosis. Parental strain BALB/cJ is susceptible to hepatic fibrosis whereas parental strain A/Jis resistant. A significant locus at 21.5 cM on mouse Chromosome 15 was identified and named Hfib1. Hfib1 gives a peak LOD score of 4.0 at D15Mit122. BALB/cJ-derived alleles confer recessively inherited susceptibility to hepatic fibrosis at Hfib1.

References
Original:  J:80619 Hillebrandt S, et al., Genome-wide analysis of hepatic fibrosis in inbred mice identifies the susceptibility locus Hfib1 on chromosome 15. Gastroenterology. 2002 Dec;123(6):2041-51
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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
11/12/2024
MGI 6.24
The Jackson Laboratory