A DBA/2 x D2B6F(1) backcross was produced in order to study the genetic bac
kground of pathological soft tissue calcification in the mouse. Calcificati
on was assessed in the myocardium, kidney and tongue. Significant co-segreg
ation was found with the genotype of microsatellite markers on the proximal
end of Chromosome 7. This region contains a candidate gene, Hrc, coding fo
r the histidine-rich calcium binding protein in the sarcoplasmatic reticulu
m. The results support the hypothesis that the gene previously reported to
be responsible for DCC (dystrophic cardiac calcification) in C3H mice (1) c
auses generalized soft tissue calcification in DBA/2 mice. (C) 1998 Academi
c Press.