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GENE - TERM ANNOTATION REPORT

RGD ID: 18906070
Species: Heterocephalus glaber
RGD Object: Gene
Symbol: Fip1l1
Name: factor interacting with PAPOLA and CPSF1
Acc ID: DOID:999
Term: hypereosinophilic syndrome
Definition: A leukocyte disease that is characterized by high numbers of eosinophils which over time enter various tissues, eventually damaging organs. (DO)
Definition Source(s): https://en.wikipedia.org/wiki/Hypereosinophilic_syndrome "DO" "DO", https://www.mayoclinic.org/diseases-conditions/hypereosinophilic-syndrome/symptoms-causes/syc-20352854 "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)
Fip1l1 ISOFIP1L1 (Homo sapiens)9068941CTDCTD Direct Evidence: marker/mechanismPMID:16778211 PMID:28347583 PMID:31036733
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