Noonan syndrome 3

Summary
Synonym
  • NS3
Definition
A Noonan syndrome that has_material_basis_in heterozygous mutation in the KRAS gene.
Super Class
Noonan syndrome autosomal dominant disease
External Links
Disease Ontology
DOID:0060581
Mondo Disease Ontology
MeSH
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying entries 11 - 20 of 35 in total
Gene ID Gene Symbol Description Source
1634 DCN decorin
2348 FOLR1 folate receptor alpha
2597 GAPDH glyceraldehyde-3-phosphate dehydrogenase
2653 GCSH glycine cleavage system protein H
2720 GLB1 galactosidase beta 1
2731 GLDC glycine decarboxylase
2821 GPI glucose-6-phosphate isomerase
3339 HSPG2 heparan sulfate proteoglycan 2
4968 OGG1 8-oxoguanine DNA glycosylase
5224 PGAM2 phosphoglycerate mutase 2

About Release Notes Help Feedback

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024