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Pfibs2BALB/c
QTL Variant Detail
Summary
QTL variant: Pfibs2BALB/c
Name: pulmonary fibrosis susceptibility 2; BALB/c
MGI ID: MGI:3033795
QTL: Pfibs2  Location: unknown  Genetic Position: Chr13, Syntenic
Variant
origin
Strain of Specimen:  BALB/c
Variant
description
Allele Type:    QTL
Notes

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

J:75407

Inbred mouse strain (DBA/2) is highly susceptible to bleomycin-induced pulmonary fibrosis and is genetically very dissimilar to the standard fibrosis-sensitive strain, C57BL/6. The strain difference enabled the authors to genetically map the loci underlying the phenotype. One marker named Pfibs1, mapped within a region of mouse Chromosome 6 that contains a cluster of genes that are members of the tumor necrosis factor (TNF)-receptor family. A second locus, Pfibs2 mapped within a region of mouse Chromosome 13 that included the Fgf gene family.

References
Original:  J:75407 Barth RK, et al., Mapping susceptibility genes for the induction of pulmonary fibrosis in mice. Chest. 2002 Mar;121(3 Suppl):21S
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
11/05/2024
MGI 6.24
The Jackson Laboratory