polycystic kidney disease 2

Summary
Synonym
  • Apkd2
  • Pkd2
  • Polycystic Kidney Disease, Adult, Type II
Definition
A autosomal dominant polycystic kidney disease that has_material_basis_in autosomal dominant inheritance of mutation in the PKD2 gene on chromosome 4q22.1.
Super Class
autosomal dominant polycystic kidney disease
Disease Ontology
DOID:0110859
Mondo Disease Ontology
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
5311 PKD2 polycystin 2, transient receptor potential cation channel
9033 PKD2L1 polycystin 2 like 1, transient receptor potential cation channel
27039 PKD2L2 polycystin 2 like 2, transient receptor potential cation channel
Displaying all 3 entries
Gene ID Gene Symbol Description Source
18764 Pkd2 polycystin 2, transient receptor potential cation channel
53871 Pkd2l2 polycystic kidney disease 2-like 2
329064 Pkd2l1 polycystic kidney disease 2-like 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
432387 pkd2 polycystic kidney disease 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
178424 pkd-2 Polycystin-2
The Human Phenotype Ontology
Displaying entries 41 - 42 of 42 in total
HPO ID HPO Term
HP:0003829 Typified by incomplete penetrance
HP:0002240 Hepatomegaly
Displaying all 5 entries
Gene ID Gene Symbol Description
23193 GANAB glucosidase II alpha subunit
29880 ALG5 ALG5 dolichyl-phosphate beta-glucosyltransferase
5310 PKD1 polycystin 1, transient receptor potential channel interacting
5311 PKD2 polycystin 2, transient receptor potential cation channel
79796 ALG9 ALG9 alpha-1,2-mannosyltransferase

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024