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GENE - TERM ANNOTATION REPORT

RGD ID: 1321899
Species: Homo sapiens
RGD Object: Gene
Symbol: RRAS2
Name: RAS related 2
Acc ID: DOID:3490
Term: Noonan syndrome
Definition: A RASopathy that is characterized by mildly unusual facial features, short stature, heart defects, bleeding problems, skeletal malformations, and many other signs and symptoms. (DO)
Definition Source(s): https://ghr.nlm.nih.gov/condition/noonan-syndrome#definition "DO" "DO", https://rarediseases.info.nih.gov/diseases/10955/noonan-syndrome "DO" "DO", https://research.nhgri.nih.gov/atlas/condition/noonan-syndrome "DO" "DO", https://www.genome.gov/Genetic-Disorders/Noonan-Syndrome "DO" "DO"
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction is comprised of a complex set of reactions and/or regulatory events, possibly involving additional chemicals and/or gene products.
Object SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
RRAS2 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Noonan syndromePMID:25741868
RRAS2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Noonan syndromePMID:25741868 PMID:31130282
RRAS2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Noonan syndromePMID:25741868 PMID:28492532 PMID:31130282 PMID:31130285
RRAS2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Noonan syndromePMID:25741868 PMID:31130282 PMID:31130285 PMID:8052619
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