Mouse Genome Informatics
hm
    Pkd1tm2.1Ggg/Pkd1tm2.1Ggg
involves: 129S4/SvJae * Black Swiss * C57BL/6
Key:
phenotype observed in females WTSI Wellcome Trust Sanger Institute
phenotype observed in males EuPh Europhenome
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 IDRef(s)
Polycystic Kidney Disease 1; PKD1 173900 J:103719