About   Help   FAQ
Phenotypes Associated with This Genotype
Genotype
MGI:3617390
Allelic
Composition
Pkd1tm2.1Ggg/Pkd1tm2.1Ggg
Genetic
Background
involves: 129S4/SvJae * Black Swiss * C57BL/6
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Pkd1tm2.1Ggg mutation (0 available); any Pkd1 mutation (68 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
mortality/aging
• stage not specified, although embryos are recovered at E15.5

renal/urinary system

endocrine/exocrine glands

homeostasis/metabolism
• phenotype is stated to be similar to that of compound heterozygous Pkd1tm1Ggg and Pkd1tm2.1Ggg mice, however no data is presented in J:103719

cardiovascular system
• phenotype is stated to be similar to that of compound heterozygous Pkd1tm1Ggg and Pkd1tm2.1Ggg mice, however no data is presented in J:103719

Mouse Models of Human Disease
OMIM ID Ref(s)
Polycystic Kidney Disease 1; PKD1 173900 J:103719


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
09/13/2016
MGI 6.05
The Jackson Laboratory