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GENE - TERM ANNOTATION REPORT

RGD ID: 736654
Species: Mus musculus
RGD Object: Gene
Symbol: Galr2
Name: galanin receptor 2
Acc ID: DOID:9008627
Term: Severe Congenital Neutropenia 10
Definition: Infantile onset of neutropenia, which may be associated with bacterial infections, including skin abscesses. Caused by compound heterozygous mutation in the SRP68 gene on chromosome 17q25.
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)
Galr2 ISOGALR2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Neutropenia, severe congenital, 10, autosomal recessivePMID:32273475
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