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Standards Ontologies Notations
nephrotic syndrome type 16

Summary
Definition
A familial nephrotic syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the KANK2 gene on chromosome 19p13.
Super Class
autosomal recessive disease familial nephrotic syndrome
Disease Ontology
DOID:0080272
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
25959 KANK2 KN motif and ankyrin repeat domains 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
235041 Kank2 KN motif and ankyrin repeat domains 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
100361376 Kank2 KN motif and ankyrin repeat domains 2
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International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

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