Noonan syndrome 4

Summary
Synonym
  • NS4
Definition
A Noonan syndrome that has_material_basis_in heterozygous mutation in the SOS1 gene on chromosome 2p22.
Super Class
Noonan syndrome autosomal dominant disease
Disease Ontology
DOID:0060582
Mondo Disease Ontology
MeSH
OMIM
MGI genotype (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
6654 SOS1 SOS Ras/Rac guanine nucleotide exchange factor 1
Displaying 1 entry
Gene ID Gene Symbol Description Source
851019 CDC25 Ras family guanine nucleotide exchange factor CDC25
The Human Phenotype Ontology
Displaying entries 21 - 30 of 70 in total
HPO ID HPO Term
HP:0000639 Nystagmus
HP:0000767 Pectus excavatum
HP:0000768 Pectus carinatum
HP:0000938 Osteopenia
HP:0000978 Bruising susceptibility
HP:0000995 Melanocytic nevus
HP:0001004 Lymphedema
HP:0001156 Brachydactyly
HP:0001249 Intellectual disability
HP:0001252 Hypotonia
Displaying all 2 entries
Gene ID Gene Symbol Description
3845 KRAS KRAS proto-oncogene, GTPase
4893 NRAS NRAS proto-oncogene, GTPase

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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