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GENE - TERM ANNOTATION REPORT

RGD ID: 1564481
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Atp11c
Name: ATPase phospholipid transporting 11C
Acc ID: DOID:12259
Term: hemophilia B
Definition: A blood coagulation disease that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait. (DO)
Definition Source(s): http://www.nlm.nih.gov/medlineplus/ency/article/000539.htm "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)
Atp11c ISOATP11C (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Hereditary factor IX deficiency diseasePMID:2198809 PMID:24375831 PMID:28492532 PMID:3029178 PMID:4045960 PMID:8304338
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