Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1


  • An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1
  • Curation Notes: ClinVar Annotator: match by OMIM:612286
  • Original References(s): PMID:12324554


  • An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1
  • Curation Notes: ClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemic, 1
  • Original References(s): PMID:25741868


  • An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1
  • Curation Notes: ClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemic, 1
  • Original References(s): PMID:28492532


  • An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1
  • Curation Notes: ClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemic, 1
  • Original References(s): PMID:24033266


  • An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1
  • Curation Notes: ClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemic, 1


  • An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1
  • Curation Notes: ClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemic, 1
  • Original References(s): PMID:25082825 PMID:26272126


  • An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1
  • Curation Notes: ClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemic, 1
  • Original References(s): PMID:16688119 PMID:28492532 PMID:28893421


  • An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1
  • Curation Notes: ClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemic, 1
  • Original References(s): PMID:26047794 PMID:27378183


  • An association has been curated linking Slc34a1 and hypophosphatemic nephrolithiasis/osteoporosis 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for ClinVar variants, variant-to-disease annotations and gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with SLC34A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to hypophosphatemic nephrolithiasis/osteoporosis 1  (DOID:0080077)
  • 75 papers in RGD have been used to annotate Slc34a1
  • Curation Notes: ClinVar Annotator: match by term: Nephrolithiasis/osteoporosis, hypophosphatemic, 1
  • Original References(s): PMID:26047794


  • Go Back to source page   Continue to Ontology report