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GENE - TERM ANNOTATION REPORT

RGD ID: 620622
Species: Rattus norvegicus
RGD Object: Gene
Symbol: Slc26a2
Name: solute carrier family 26 member 2
Acc ID: DOID:0050648
Term: atelosteogenesis
Definition: An osteochondrodysplasia that is characterized by specific patterns of aplasia/hypoplasia of humeri, femora, spine in newborns. (DO)
Definition Source(s): https://link.springer.com/chapter/10.1007/978-1-60327-161-5_17 "DO" "DO", https://rarediseases.info.nih.gov/diseases/9287/atelosteogenesis-type-1 "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)
Slc26a2 ISOSLC26A2 (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Atelosteogenesis 
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