Symbol Name ID |
Pkd2
polycystin 2, transient receptor potential cation channel MGI:1099818 |
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 |
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Availability | Mouse Genotype | |||||||||||
Pkd2tm1Dwo/Pkd2tm1Dwo | ||||||||||||
Pkd2tm1Gwu/Pkd2tm1Gwu | ||||||||||||
Pkd2tm1Som/Pkd2tm1Som | ||||||||||||
Pkd2tm1Som/Pkd2tm2Som | ||||||||||||
Pkd2tm2Som/Pkd2+ | ||||||||||||
Pkd2tm1.1Gwu/Pkd2tm1.1Gwu Tg(Vil1-cre)997Gum/0 (conditional) |
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 04/23/2024 MGI 6.23 |
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