Noonan syndrome 9

Summary
Synonym
  • NS9
Definition
A Noonan syndrome that has_material_basis_in heterozygous mutation in the SOS2 gene on chromosome 14q21.
Super Class
Noonan syndrome autosomal dominant disease
Disease Ontology
DOID:0060587
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6655 SOS2 SOS Ras/Rho guanine nucleotide exchange factor 2
Displaying 1 entry
Gene ID Gene Symbol Description Source
851019 CDC25 Ras family guanine nucleotide exchange factor CDC25
The Human Phenotype Ontology
Displaying entries 11 - 20 of 70 in total
HPO ID HPO Term
HP:0000078 Abnormality of the genital system
HP:0000476 Cystic hygroma
HP:0000325 Triangular face
HP:0000494 Downslanted palpebral fissures
HP:0000348 High forehead
HP:0000218 High palate
HP:0000465 Webbed neck
HP:0000508 Ptosis
HP:0000520 Proptosis
HP:0000635 Blue irides
Displaying all 2 entries
Gene ID Gene Symbol Description
3845 KRAS KRAS proto-oncogene, GTPase
4893 NRAS NRAS proto-oncogene, GTPase

About Release Notes Help Feedback

Click here to visit the beta site.


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 v4.1.0

Last updated: December 9, 2024