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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:0070183
Term: spermatogenic failure 5
Definition: A spermatogenic failure that is characterized by autosomal recessive inheritance of large-headed, multiflagellar, polyploid spermatozoa that has_material_basis_in mutation in the AURKC gene on chromosome 19q13. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/17435757 "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: Male infertility with spermatogenesis disorderPMID:25741868 PMID:26781211 PMID:28332357 PMID:28492532
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