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Standards Ontologies Notations
CAKUT1

Summary
Synonym
  • Congenital anomalies of the kidney and urinary tract 1
Definition
A CAKUT that has_material_basis_in heterozygous mutation in the DSTYK gene on chromosome 1q32.
Super Class
CAKUT
Disease Ontology
DOID:0080206
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
25778 DSTYK dual serine/threonine and tyrosine protein kinase
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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