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GENE - TERM ANNOTATION REPORT

RGD ID: 1321547
Species: Homo sapiens
RGD Object: Gene
Symbol: DGCR2
Name: DiGeorge syndrome critical region gene 2
Acc ID: DOID:11198
Term: DiGeorge syndrome
Definition: A syndrome that has_material_basis_in a large deletion of the chromosome 22q11.2 region which includes the DGS gene needed for development of the thymus and related glands with subsequent lack of T-cell production. (DO)
Definition Source(s): http://www.ncbi.nlm.nih.gov/bookshelf/br.fcgi?book=gnd&part=digeorgesyndrome "DO" "DO", https://ghr.nlm.nih.gov/condition/22q112-deletion-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)
DGCR2 EXP 11554173CTDCTD Direct Evidence: marker/mechanism 
DGCR2 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: DiGeorge syndromePMID:31690835
DGCR2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: DiGeorge syndromePMID:24826987 PMID:25205790 PMID:25516202 PMID:25860641 PMID:26805781 PMID:26805782 PMID:28492532 PMID:29500247 PMID:30245509
DGCR2 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: DiGeorge syndromePMID:24826987 PMID:25205790 PMID:25516202 PMID:28492532
DGCR2 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: DiGeorge syndromePMID:21921585 PMID:25516202 PMID:28492532
DGCR2 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: DiGeorge syndromePMID:28492532
DGCR2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: DiGeorge syndromePMID:32581362
DGCR2 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: DiGeorge syndrome 
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