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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking SLC6A19 and iminoglycinuria in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:34891254 (Homo sapiens)
  • 4 RGD objects have been annotated to iminoglycinuria  (DOID:0112265)
  • 4 papers in RGD have been used to annotate SLC6A19
  • Curation Notes: ClinVar Annotator: match by term: Iminoglycinuria
  • Original References(s): PMID:15286787 PMID:15286788 PMID:18484095 PMID:19472175 PMID:25741868 PMID:28492532 PMID:28924877


    • An association has been curated linking SLC6A19 and iminoglycinuria in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:15157137|RGD:152114733|RGD:38457283 (Homo sapiens) & RGD:15157137|RGD:152114733|RGD:38457283 (Homo sapiens) & RGD:15157137|RGD:152114733|RGD:38457283 (Homo sapiens)
  • 4 RGD objects have been annotated to iminoglycinuria  (DOID:0112265)
  • 4 papers in RGD have been used to annotate SLC6A19
  • Curation Notes: ClinVar Annotator: match by term: Iminoglycinuria
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SLC6A19 and iminoglycinuria in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:8595590 (Homo sapiens)
  • 4 RGD objects have been annotated to iminoglycinuria  (DOID:0112265)
  • 4 papers in RGD have been used to annotate SLC6A19
  • Curation Notes: ClinVar Annotator: match by term: Iminoglycinuria
  • Original References(s): PMID:15286788 PMID:17555458 PMID:18484095 PMID:19185582 PMID:21814048 PMID:24033266 PMID:25741868 PMID:28492532 PMID:35606766


    • An association has been curated linking SLC6A19 and iminoglycinuria in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13480008 (Homo sapiens)
  • 4 RGD objects have been annotated to iminoglycinuria  (DOID:0112265)
  • 4 papers in RGD have been used to annotate SLC6A19
  • Curation Notes: ClinVar Annotator: match by term: Iminoglycinuria
  • Original References(s): PMID:15286787 PMID:15286788 PMID:16199547 PMID:18484095 PMID:25741868 PMID:28492532


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