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GENE - TERM ANNOTATION REPORT

RGD ID: 14272498
Species: Sus scrofa
RGD Object: Gene
Symbol: TTN
Name: titin
Acc ID: DOID:2843
Term: long QT syndrome
Definition: An autosomal genetic disease that is characterized by delayed repolarization of the heart following a heartbeat increases the risk of episodes of torsade de pointes (TDP, a form of irregular heartbeat that originates from the ventricles). (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Long_QT_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)
TTN ISOTTN (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Congenital long QT syndrome | ClinVar Annotator: match by term: Long QT syndromePMID:17344846 PMID:23861362 PMID:24033266 PMID:25145518 PMID:25741868 PMID:26467025 PMID:26516846 PMID:26567375 PMID:27930701 PMID:28135719 PMID:28492532 PMID:29253866 PMID:31785789 PMID:37091313
TTN ISOTTN (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Congenital long QT syndrome | ClinVar Annotator: match by term: Long QT syndromePMID:17344846 PMID:23861362 PMID:24033266 PMID:25145518 PMID:25741868 PMID:26467025 PMID:26567375 PMID:27854218 PMID:27930701 PMID:28492532 PMID:29253866
TTN ISOTTN (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Congenital long QT syndrome | ClinVar Annotator: match by term: Long QT syndromePMID:17344846 PMID:23861362 PMID:24033266 PMID:25145518 PMID:25741868 PMID:26467025 PMID:26567375 PMID:27930701 PMID:28492532 PMID:29253866
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