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GENE - TERM ANNOTATION REPORT

RGD ID: 727960
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Hax1
Name: HCLS1 associated protein X-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)
Hax1 ISOHAX1 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Inborn genetic diseasesPMID:17187068 PMID:18337561 PMID:19036076 PMID:20065084 PMID:20177699 PMID:20220065 PMID:22102707 PMID:24482108 PMID:25741868 PMID:28492532 PMID:32005694 PMID:33381479 PMID:34134972 PMID:34826056
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