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CRRD ID: 1345405
Species: Homo sapiens
CRRD Object: Gene
Symbol: ETV6
Name: ETS variant transcription factor 6
Acc ID: DOID:630
Term: genetic disease
Definition: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
Definition Source(s): MESH:D030342,
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.
QualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
 IAGPRGD:135314228554872ClinVarClinVar Annotator: match by term: Inborn genetic diseases

PMID:19570513, PMID:19854944, PMID:20400516, PMID:20412772, PMID:20517297, PMID:22162831, PMID:23276184, PMID:25581430, PMID:25807284, PMID:26102509, PMID:26522332, PMID:7795247, PMID:8481506, PMID:9250681
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RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.