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GENE - TERM ANNOTATION REPORT

RGD ID: 1563858
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Hesx1
Name: HESX homeobox 1
Acc ID: DOID:630
Term: genetic disease
Definition: A disease that has_material_basis_in genetic variations in the human genome. (DO)
Definition Source(s): http://ghr.nlm.nih.gov/ "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)
Hesx1 ISOHESX1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:11136712 PMID:17315526 PMID:17576681 PMID:19093031 PMID:22145475 PMID:23465708 PMID:25500790 PMID:25741868 PMID:27000987 PMID:28492532 PMID:30266296 PMID:32483926 PMID:33098107 PMID:9536098 PMID:9620767
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