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Standards Ontologies Notations
CAKUT

Summary
Synonym
  • Congenital anomalies of the kidney and urinary tract
  • Renal or urinary tract malformation
Definition
A urinary system disease characterized by structural malformations in the kidney and/or urinary tract containing vesicoureteral reflux.
Super Class
urinary system disease
Disease Ontology
DOID:0080205
Mondo Disease Ontology
MeSH
ORDO
OMIM
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying all 4 entries
Gene ID Gene Symbol Description Source
652 BMP4 bone morphogenetic protein 4
3304 HSPA1B heat shock protein family A (Hsp70) member 1B
3977 LIFR LIF receptor subunit alpha
8204 NRIP1 nuclear receptor interacting protein 1
Displaying all 3 entries
Gene ID Gene Symbol Description Source
12159 Bmp4 bone morphogenetic protein 4
16880 Lifr LIF receptor alpha
193740 Hspa1a heat shock protein 1A
Displaying all 2 entries
Gene ID Gene Symbol Description Source
24472 Hspa1a heat shock protein family A (Hsp70) member 1A
81680 Lifr LIF receptor subunit alpha
Displaying 1 entry
Gene ID Gene Symbol Description Source
33432 dpp decapentaplegic
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
399322 bmp4.S bone morphogenetic protein 4 S homeolog Xenopus laevis (African clawed frog)
Displaying 1 entry
Gene ID Gene Symbol Description Source
179068 dbl-1 Protein dbl-1
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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