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GENE - TERM ANNOTATION REPORT

RGD ID: 736378
Species: Homo sapiens
RGD Object: Gene
Symbol: APOE
Name: apolipoprotein E
Acc ID: DOID:0080666
Term: warfarin sensitivity
Definition: An inherited metabolic disorder that is characterized by a low tolerance for the drug warfarin. (DO)
Definition Source(s): https://ghr.nlm.nih.gov/condition/warfarin-sensitivity#inheritance "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)
APOE IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Warfarin sensitivity 
APOE IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Warfarin sensitivity 
APOE IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Warfarin sensitivity 
APOE IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Warfarin sensitivityPMID:16103896 PMID:16143024 PMID:17289397 PMID:19667110 PMID:20031551 PMID:20031582 PMID:22992668 PMID:25741868 PMID:2992507 PMID:3243553 PMID:6300187 PMID:9649566
APOE IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Warfarin sensitivityPMID:10213549 PMID:10799751 PMID:11835377 PMID:11940689 PMID:11940706 PMID:14741101 PMID:15048896 PMID:15146461 PMID:15184602 PMID:15326261 PMID:15557508 PMID:15668424 PMID:18338393 PMID:18979180 PMID:18987351 PMID:19605830 PMID:19846850 PMID:21742527 PMID:22381401 PMID:23060451 PMID:23296339 PMID:23571587 PMID:24033266 PMID:25741868 PMID:27260402 PMID:29842932 PMID:2987927 PMID:32376954 PMID:3353383 PMID:3922972 PMID:7263700 PMID:8294487 PMID:8346443 PMID:8350998 PMID:8618665 PMID:8644717 PMID:9343467 PMID:9932938
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