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GENE - TERM ANNOTATION REPORT

RGD ID: 1347029
Species: Homo sapiens
RGD Object: Gene
Symbol: MIR26A1
Name: microRNA 26a-1
Acc ID: DOID:9008496
Term: Visceral Heterotaxy 4, Autosomal
Definition: This disease is a developmental condition characterized by randomization of the placement of visceral organs, including the heart, lungs, liver, spleen, and stomach. The organs are oriented randomly with respect to the left-right axis and with respect to one another.
Definition Source(s): OMIM:613751
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)
MIR26A1 IAGP (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Heterotaxy, visceral, 4, autosomalPMID:28492532
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