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GENE - TERM ANNOTATION REPORT

RGD ID: 733686
Species: Homo sapiens
RGD Object: Gene
Symbol: SLC34A1
Name: solute carrier family 34 member 1
Acc ID: DOID:0080655
Term: hypophosphatemic nephrolithiasis/osteoporosis
Definition: A kidney disease that is characterized by formation of renal calcium\nstones or bone demineralization. (DO)
Definition Source(s): https://www.nejm.org/doi/full/10.1056/NEJMoa020028 "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)
SLC34A1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemicPMID:24033266 PMID:25741868 PMID:28492532
SLC34A1 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemic 
SLC34A1 IAGP (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemicPMID:25050900 PMID:28492532 PMID:30943683
SLC34A1 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemicPMID:28492532
SLC34A1 IAGP (Homo sapiens) or (Homo sapiens) or (Homo sapiens)8554872ClinVarClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemicPMID:25741868 PMID:28492532
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