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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

An association has been curated linking LOC130055850 and Hereditary Paraganglioma-Pheochromocytoma Syndromes 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:14714108 (Homo sapiens)
  • 20 RGD objects have been annotated to Hereditary Paraganglioma-Pheochromocytoma Syndromes  (DOID:9005607)
  • 0 papers in RGD have been used to annotate LOC130055850
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paraganglioma-Pheochromocytoma Syndromes
  • Original References(s): PMID:21685915 PMID:22452945 PMID:26070438 PMID:28492532


    • An association has been curated linking LOC130055850 and Hereditary Paraganglioma-Pheochromocytoma Syndromes 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:25328114 (Homo sapiens)
  • 20 RGD objects have been annotated to Hereditary Paraganglioma-Pheochromocytoma Syndromes  (DOID:9005607)
  • 0 papers in RGD have been used to annotate LOC130055850
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paraganglioma-Pheochromocytoma Syndromes
  • Original References(s): PMID:21685915 PMID:26070438 PMID:28492532


    • An association has been curated linking LOC130055850 and Hereditary Paraganglioma-Pheochromocytoma Syndromes 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:150333283 (Homo sapiens)
  • 20 RGD objects have been annotated to Hereditary Paraganglioma-Pheochromocytoma Syndromes  (DOID:9005607)
  • 0 papers in RGD have been used to annotate LOC130055850
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paraganglioma-Pheochromocytoma Syndromes
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking LOC130055850 and Hereditary Paraganglioma-Pheochromocytoma Syndromes 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:11621766 (Homo sapiens)
  • 20 RGD objects have been annotated to Hereditary Paraganglioma-Pheochromocytoma Syndromes  (DOID:9005607)
  • 0 papers in RGD have been used to annotate LOC130055850
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paraganglioma-Pheochromocytoma Syndromes
  • Original References(s): PMID:22452945 PMID:25741868 PMID:26070438 PMID:28492532 PMID:34130653


    • An association has been curated linking LOC130055850 and Hereditary Paraganglioma-Pheochromocytoma Syndromes 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:597924184 (Homo sapiens)
  • 20 RGD objects have been annotated to Hereditary Paraganglioma-Pheochromocytoma Syndromes  (DOID:9005607)
  • 0 papers in RGD have been used to annotate LOC130055850
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paraganglioma-Pheochromocytoma Syndromes
  • Original References(s): PMID:21685915 PMID:22452945 PMID:28492532 PMID:30877234


    • An association has been curated linking LOC130055850 and Hereditary Paraganglioma-Pheochromocytoma Syndromes 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:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens) & RGD:126749183|RGD:127250127|RGD:127325794|RGD:12883079|RGD:12889995|RGD:13480633|RGD:13496036|RGD:13501209|RGD:13607297|RGD:13607306|RGD:15140258|RGD:151735583|RGD:151786878|RGD:152065437|RGD:152081676|RGD:152091350|RGD:152095803|RGD:152130193|RGD:155692542|RGD:156059984|RGD:156130864|RGD:156345579|RGD:25317181|RGD:26914135|RGD:405074375|RGD:405078386|RGD:597861899|RGD:597906962|RGD:597947088 (Homo sapiens)
  • 20 RGD objects have been annotated to Hereditary Paraganglioma-Pheochromocytoma Syndromes  (DOID:9005607)
  • 0 papers in RGD have been used to annotate LOC130055850
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paraganglioma-Pheochromocytoma Syndromes
  • Original References(s): PMID:28492532


    • An association has been curated linking LOC130055850 and Hereditary Paraganglioma-Pheochromocytoma Syndromes 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:13496532 (Homo sapiens)
  • 20 RGD objects have been annotated to Hereditary Paraganglioma-Pheochromocytoma Syndromes  (DOID:9005607)
  • 0 papers in RGD have been used to annotate LOC130055850
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paraganglioma-Pheochromocytoma Syndromes
  • Original References(s): PMID:26467025 PMID:28492532


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