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GENE - TERM ANNOTATION REPORT

RGD ID: 735504
Species: Homo sapiens
RGD Object: Gene
Symbol: C3
Name: complement C3
Acc ID: DOID:630
Term: genetic disease
Definition: A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/ "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)
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:25741868 PMID:28492532
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:28492532
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases 
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:16687714 PMID:17634448 PMID:17767156 PMID:19259132 PMID:1976733 PMID:20664795 PMID:21576320 PMID:22718507 PMID:23112567 PMID:23455636 PMID:25741868 PMID:28492532 PMID:7870343
C3 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:17634448 PMID:18325906 PMID:19168221 PMID:1976733 PMID:25741868 PMID:28492532
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