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GENE - TERM ANNOTATION REPORT

9 Annotations Found.

An association has been curated linking NRAS and Myelodysplasia 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:9688997 (Homo sapiens)
  • 128 RGD objects have been annotated to Myelodysplasia  (HP:0002863)
  • 35 papers in RGD have been used to annotate NRAS
  • Curation Notes: ClinVar Annotator: match by term: Myelodysplastic syndrome
  • Original References(s): PMID:10598665 PMID:12460918 PMID:16273091 PMID:16291983 PMID:16434492 PMID:16518851 PMID:17384584 PMID:17671181 PMID:17699718 PMID:17823240 PMID:18390968 PMID:18794081 PMID:19047918 PMID:19657110 PMID:19966803 PMID:20130576 PMID:20179705 PMID:20619739 PMID:20736745 PMID:21263000 PMID:21305640 PMID:21729679 PMID:21829508 PMID:22220252 PMID:23325582 PMID:23414587 PMID:23708912 PMID:24806883 PMID:25157968 PMID:25741868 PMID:26619011 PMID:2674680 PMID:26980726 PMID:27069254 PMID:27121720 PMID:27276561 PMID:28098151 PMID:28492532 PMID:28594414 PMID:29692343 PMID:8120410


    • An association has been curated linking NRAS and Myelodysplasia 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:12834338 (Homo sapiens)
  • 128 RGD objects have been annotated to Myelodysplasia  (HP:0002863)
  • 35 papers in RGD have been used to annotate NRAS
  • Curation Notes: ClinVar Annotator: match by term: Myelodysplastic syndrome
  • Original References(s): PMID:16291983 PMID:18390968 PMID:19657110 PMID:20130576 PMID:20179705 PMID:23414587 PMID:25157968 PMID:26619011 PMID:2674680 PMID:8120410


    • An association has been curated linking NRAS and Myelodysplasia 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:9831519 (Homo sapiens)
  • 128 RGD objects have been annotated to Myelodysplasia  (HP:0002863)
  • 35 papers in RGD have been used to annotate NRAS
  • Curation Notes: ClinVar Annotator: match by term: Myelodysplastic syndrome
  • Original References(s): PMID:12460918 PMID:16273091 PMID:16291983 PMID:16434492 PMID:17699718 PMID:18390968 PMID:18948947 PMID:19075190 PMID:19657110 PMID:20130576 PMID:20179705 PMID:20619739 PMID:20736745 PMID:21305640 PMID:21729679 PMID:21829508 PMID:22407852 PMID:2278970 PMID:23414587 PMID:23515407 PMID:23614898 PMID:25157968 PMID:26619011 PMID:2674680 PMID:3122217 PMID:8120410


    • An association has been curated linking NRAS and Myelodysplasia 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:8591584 (Homo sapiens)
  • 128 RGD objects have been annotated to Myelodysplasia  (HP:0002863)
  • 35 papers in RGD have been used to annotate NRAS
  • Curation Notes: ClinVar Annotator: match by term: Myelodysplastic syndrome
  • Original References(s): PMID:16291983 PMID:18390968 PMID:18633438 PMID:20130576 PMID:20179705 PMID:22962325 PMID:23414587 PMID:25157968 PMID:25741868 PMID:26619011 PMID:2674680 PMID:3102434 PMID:8120410


    • An association has been curated linking NRAS and Myelodysplasia 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:8563955 (Homo sapiens)
  • 128 RGD objects have been annotated to Myelodysplasia  (HP:0002863)
  • 35 papers in RGD have been used to annotate NRAS
  • Curation Notes: ClinVar Annotator: match by term: Myelodysplastic syndrome
  • Original References(s): PMID:16291983 PMID:17332249 PMID:17517660 PMID:18375819 PMID:18390968 PMID:19657110 PMID:19775298 PMID:20130576 PMID:20179705 PMID:21079152 PMID:23414587 PMID:23431193 PMID:2407301 PMID:25157968 PMID:25741868 PMID:26619011 PMID:2674680 PMID:27993330 PMID:2989702 PMID:8120410


    • An association has been curated linking NRAS and Myelodysplasia 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:8604307 (Homo sapiens)
  • 128 RGD objects have been annotated to Myelodysplasia  (HP:0002863)
  • 35 papers in RGD have been used to annotate NRAS
  • Curation Notes: ClinVar Annotator: match by term: Myelodysplastic syndrome
  • Original References(s): PMID:12460918 PMID:16273091 PMID:16291983 PMID:16434492 PMID:17332249 PMID:17699718 PMID:18390968 PMID:18948947 PMID:19075190 PMID:19657110 PMID:20130576 PMID:20179705 PMID:20619739 PMID:20736745 PMID:21305640 PMID:21586752 PMID:21729679 PMID:21829508 PMID:22144181 PMID:22407852 PMID:22499344 PMID:2278970 PMID:23414587 PMID:23515407 PMID:24284627 PMID:25157968 PMID:25741868 PMID:26619011 PMID:2674680 PMID:28098151 PMID:28492532 PMID:28594414 PMID:3122217 PMID:8120410


    • An association has been curated linking NRAS and Myelodysplasia 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:9831520 (Homo sapiens)
  • 128 RGD objects have been annotated to Myelodysplasia  (HP:0002863)
  • 35 papers in RGD have been used to annotate NRAS
  • Curation Notes: ClinVar Annotator: match by term: Myelodysplastic syndrome
  • Original References(s): PMID:12460918 PMID:16291983 PMID:18390968 PMID:18948947 PMID:20130576 PMID:20179705 PMID:23134356 PMID:23334668 PMID:23414587 PMID:23515407 PMID:25157968 PMID:25741868 PMID:26619011 PMID:2674680 PMID:28594414 PMID:30417923 PMID:32888943 PMID:8120410


    • An association has been curated linking NRAS and Myelodysplasia 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:8607387 (Homo sapiens)
  • 128 RGD objects have been annotated to Myelodysplasia  (HP:0002863)
  • 35 papers in RGD have been used to annotate NRAS
  • Curation Notes: ClinVar Annotator: match by term: Myelodysplastic syndrome
  • Original References(s): PMID:14982869 PMID:15046639 PMID:15831708 PMID:16273091 PMID:16291983 PMID:17699718 PMID:18390968 PMID:18952898 PMID:19657110 PMID:20130576 PMID:20179705 PMID:20619739 PMID:20736745 PMID:21263000 PMID:21305640 PMID:21729679 PMID:21829508 PMID:23414587 PMID:24033266 PMID:25157968 PMID:26619011 PMID:2674680 PMID:28098151 PMID:28492532 PMID:28594414 PMID:8120410


    • An association has been curated linking NRAS and Myelodysplasia 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:10766614 (Homo sapiens)
  • 128 RGD objects have been annotated to Myelodysplasia  (HP:0002863)
  • 35 papers in RGD have been used to annotate NRAS
  • Curation Notes: ClinVar Annotator: match by term: Myelodysplastic syndrome
  • Original References(s): PMID:12460918 PMID:15951308 PMID:16273091 PMID:16291983 PMID:17699718 PMID:18390968 PMID:18948947 PMID:20130576 PMID:20179705 PMID:20619739 PMID:20736745 PMID:21305640 PMID:21729679 PMID:21829508 PMID:23414587 PMID:23515407 PMID:25157968 PMID:25741868 PMID:26619011 PMID:2674680 PMID:28098151 PMID:28492532 PMID:28594414 PMID:8120410


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