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GENE - TERM ANNOTATION REPORT

RGD ID: 1304999
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Fam161a
Name: FAM161 centrosomal protein A
Acc ID: DOID:0080485
Term: peroxisome biogenesis disorder 11A
Definition: A Zellweger syndrome that has_material_basis_in homozygous mutation in the PEX13 gene on chromosome 2p15. (DO)
Definition Source(s): https://www.ncbi.nlm.nih.gov/pubmed/17055079 "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)
Fam161a ISOFAM161A (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Peroxisome biogenesis disorder 11A (Zellweger)PMID:28492532
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