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GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking SDHAF2 and Hereditary Neoplastic Syndromes in Canis lupus familiaris.        

  • 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 SDHAF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1482 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 0 papers in RGD have been used to annotate SDHAF2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome
  • Original References(s): PMID:16199547 PMID:17576681 PMID:19628817 PMID:20071235 PMID:21224366 PMID:21348866 PMID:21752896 PMID:22241717 PMID:22703879 PMID:23062074 PMID:23666964 PMID:24033266 PMID:24414418 PMID:24712571 PMID:25394176 PMID:25741868 PMID:26016412 PMID:26096992 PMID:26269449 PMID:26467025 PMID:28099933 PMID:28492532 PMID:29641532 PMID:30050099 PMID:30306255 PMID:31687641 PMID:32741965 PMID:32887801 PMID:33748650 PMID:36597280 PMID:6264239 PMID:6286462 PMID:9536098


  • An association has been curated linking SDHAF2 and Hereditary Neoplastic Syndromes in Canis lupus familiaris.        

  • 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 SDHAF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1482 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 0 papers in RGD have been used to annotate SDHAF2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar Annotator: match by term: Hereditary neoplastic syndrome | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary
  • Original References(s): PMID:17576681 PMID:19628817 PMID:20071235 PMID:21224366 PMID:21348866 PMID:21752896 PMID:22241717 PMID:22703879 PMID:23062074 PMID:23666964 PMID:24033266 PMID:24414418 PMID:24712571 PMID:25394176 PMID:25741868 PMID:26016412 PMID:26096992 PMID:26269449 PMID:26467025 PMID:27600092 PMID:28099933 PMID:28492532 PMID:28892078 PMID:29641532 PMID:30050099 PMID:30306255 PMID:31687641 PMID:32741965 PMID:32830346 PMID:32887801 PMID:33748650 PMID:35668420 PMID:36597280 PMID:6264239 PMID:6286462 PMID:9536098


  • An association has been curated linking SDHAF2 and Hereditary Neoplastic Syndromes in Canis lupus familiaris.        

  • 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 SDHAF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1482 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 0 papers in RGD have been used to annotate SDHAF2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome
  • Original References(s): PMID:17576681 PMID:19628817 PMID:20071235 PMID:21348866 PMID:22241717 PMID:22703879 PMID:23062074 PMID:23666964 PMID:24033266 PMID:24414418 PMID:25741868 PMID:26016412 PMID:26096992 PMID:26467025 PMID:28099933 PMID:28492532 PMID:30050099 PMID:31687641 PMID:6286462 PMID:9536098


  • An association has been curated linking SDHAF2 and Hereditary Neoplastic Syndromes in Canis lupus familiaris.        

  • 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 SDHAF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1482 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 0 papers in RGD have been used to annotate SDHAF2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary
  • Original References(s): PMID:17576681 PMID:19628817 PMID:20071235 PMID:20301715 PMID:21348866 PMID:22241717 PMID:22703879 PMID:23062074 PMID:23666964 PMID:24033266 PMID:24414418 PMID:25741868 PMID:26016412 PMID:26096992 PMID:26467025 PMID:28099933 PMID:28492532 PMID:30050099 PMID:31687641 PMID:6286462 PMID:9536098


  • An association has been curated linking SDHAF2 and Hereditary Neoplastic Syndromes in Canis lupus familiaris.        

  • 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 SDHAF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1482 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 0 papers in RGD have been used to annotate SDHAF2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar Annotator: match by term: Hereditary neoplastic syndrome | ClinVar Annotator: match by term: Neoplastic Syndromes, Hereditary
  • Original References(s): PMID:17576681 PMID:19628817 PMID:20071235 PMID:21224366 PMID:21348866 PMID:22241717 PMID:22703879 PMID:23062074 PMID:23666964 PMID:24033266 PMID:24414418 PMID:24712571 PMID:25394176 PMID:25741868 PMID:26016412 PMID:26096992 PMID:26269449 PMID:26467025 PMID:27600092 PMID:28099933 PMID:28492532 PMID:28892078 PMID:29641532 PMID:30050099 PMID:30306255 PMID:31687641 PMID:32741965 PMID:32830346 PMID:32887801 PMID:33748650 PMID:35441217 PMID:35668420 PMID:36597280 PMID:36841802 PMID:6264239 PMID:6286462 PMID:9536098


  • An association has been curated linking SDHAF2 and Hereditary Neoplastic Syndromes in Canis lupus familiaris.        

  • 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 SDHAF2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1482 RGD objects have been annotated to Hereditary Neoplastic Syndromes  (DOID:9007071)
  • 0 papers in RGD have been used to annotate SDHAF2
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Cancer Syndrome | ClinVar Annotator: match by term: Hereditary cancer-predisposing syndrome | ClinVar Annotator: match by term: Hereditary neoplastic syndrome
  • Original References(s): PMID:16199547 PMID:17576681 PMID:19628817 PMID:20071235 PMID:21224366 PMID:21348866 PMID:21752896 PMID:22241717 PMID:22703879 PMID:23062074 PMID:23666964 PMID:24033266 PMID:24414418 PMID:24712571 PMID:25394176 PMID:25741868 PMID:26016412 PMID:26096992 PMID:26269449 PMID:26467025 PMID:27600092 PMID:28099933 PMID:28492532 PMID:28892078 PMID:29641532 PMID:30050099 PMID:30306255 PMID:31687641 PMID:32741965 PMID:32830346 PMID:32887801 PMID:33748650 PMID:35668420 PMID:36597280 PMID:6264239 PMID:6286462 PMID:9536098


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