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Symbol
Name
ID
Pkd2
polycystin 2, transient receptor potential cation channel
MGI:1099818
Phenotype annotations related to cardiovascular system
Darker colors indicate more annotations
Human Phenotypes
Dextrocardia
Situs inversus totalis
Mitral valve prolapse
Aortic root aneurysm
Abnormal systemic arterial morphology
Dilatation of the cerebral artery
Hypertension
Disease(s) Associated with PKD2
autosomal dominant polycystic kidney disease
polycystic kidney disease 2

Mouse Phenotypes
abnormal placenta vasculature
abnormal placental labyrinth vasculature morphology
abnormal hepatic vein morphology
abnormal heart development
abnormal heart looping
atrial septal defect
dextrocardia
mesocardia
atrioventricular septal defect
ventricular septal defect
pericardial effusion
hemorrhage
Availability Mouse Genotype
Pkd2lrm4/Pkd2lrm4
Pkd2tm1Dwo/Pkd2tm1Dwo
Pkd2tm1Gwu/Pkd2tm1Gwu
Pkd2tm2Som/Pkd2tm2Som
Pkd2tm1.1Tjwt/Pkd2tm1.1Tjwt
Tg(Tek-cre)1Ywa/0  (conditional)
Pkd2tm1.1Tjwt/Pkd2tm1.2Tjwt
Meox2tm1(cre)Sor/Meox2+  (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)
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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory