Genopathy
Gene-Disorder Association · Article
Gene
HRAS
HRas Proto-Oncogene, GTPase
Disorder
Noonan Syndrome And Noonan-Related Syndrome
First reported 2007
Key publication · disorder Gain-of-function SOS1 mutations cause a distinctive form of Noonan syndrome.Nature genetics · 2007
Association Review

In brief

The association between HRAS (HRas Proto-Oncogene, GTPase) and Noonan Syndrome And Noonan-Related Syndrome is supported by expert-curated evidence, drawing on a single expert-curated source, which records pathogenic variants.

Sources 1
Clinical variants 24
Symptoms 0
Compounds 0
Trials 0
Publications 0
01
At a glance

Association overview

A cited synthesis of the gene–disorder association, with a clinical-actionability summary where the evidence supports one.

Request access
02
Provenance

Evidence and sources

1 source

Every contributing database and publication behind this association, with evidence type, strength, accessions and deep links.

Request access
03
HRAS

The gene

2 source summaries

A gene summary alongside the source descriptions it was distilled from.

Request access
04
Noonan Syndrome And Noonan-Related Syndrome

The disorder

3 database identifiers

The disorder’s summary, prevalence, aliases and cross-reference identifiers (OMIM, Orphanet, MONDO, ICD-10, MedGen).

Request access
05
ClinVar and variant evidence

Genetic basis

24 clinical variants

ClinVar variants reported for this pair, with disorder-specific significance, review status, molecular consequence and origin.

Request access
06
Provenance

References & sources

3 references

Every source and publication cited across this dossier, as one numbered reference list.

Request access