About   Help   FAQ
Symbol
Name
ID
Pkd2
polycystin 2, transient receptor potential cation channel
MGI:1099818
Phenotype annotations related to liver/biliary system
Darker colors indicate more annotations
Human Phenotypes
Hepatomegaly
Hepatic cysts
Polycystic liver disease
Jaundice
Disease(s) Associated with PKD2
autosomal dominant polycystic kidney disease
polycystic kidney disease 2

Mouse Phenotypes
abnormal cholangiocyte primary cilium morphology
increased cholangiocyte apoptosis
abnormal cholangiocyte morphology
bile duct proliferation
dilated bile duct
liver cyst
enlarged liver
increased liver weight
abnormal liver development
abnormal liver morphology
liver fibrosis
Availability Mouse Genotype
Pkd2tm1Dwo/Pkd2tm1Dwo
Pkd2tm1Gwu/Pkd2tm1Gwu
Pkd2tm1Som/Pkd2tm1Som
Pkd2tm1Som/Pkd2tm2Som
Pkd2tm2Som/Pkd2+
Pkd2tm1.1Gwu/Pkd2tm1.1Gwu
Tg(Vil1-cre)997Gum/0  (conditional)

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)
Citing These Resources
Funding Information
Warranty Disclaimer, Privacy Notice, Licensing, & Copyright
Send questions and comments to User Support.
last database update
04/23/2024
MGI 6.23
The Jackson Laboratory