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Phenotypes Associated with This Genotype
Genotype
MGI:5502422
Allelic
Composition
Pkd1tm1Ggg/Pkd1tm2Ggg
Tg(Col1a1-cre)1Bek/0
Genetic
Background
involves: 129S4/SvJae * CD-1
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pkd1tm1Ggg mutation (0 available); any Pkd1 mutation (153 available)
Pkd1tm2Ggg mutation (1 available); any Pkd1 mutation (153 available)
Tg(Col1a1-cre)1Bek mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype

Osteopenia in newborn Pkd1tm1Ggg/Pkd1tm2Ggg Tg(Col1a1-cre)1Bek/0 mice

mortality/aging

limbs/digits/tail
• newborns have short and less mineralized femurs

skeleton
• newborns have short and less mineralized femurs
• osteopenia is seen in newborns
• newborns show a delay in bone mineralization in calvarial and vertebral bone tissues
• bone phenotype is more severe than in Pkd1tm1Ggg/Pkd1tm1Ggg Tg(Col1a1-cre)1Bek/0 mice


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
01/06/2026
MGI 6.24
The Jackson Laboratory