Send us a Message
Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes Variants Community Projects QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Synteny Browser (VCMap) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) AllianceMine GViewer (Genome Viewer)
Aging & Age-Related Disease Cancer & Neoplastic Disease Cardiovascular Disease Coronavirus Disease Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Infectious Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models Genetic Models Autism Models Rat PhenoMiner (Quantitative Phenotypes) Chinchilla PhenoMiner Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes Phenotypes in Other Animal Models Animal Husbandry Strain Medical Records Phylogenetics Strain Availability Calendar Rats 101 Submissions Photo Archive
Pathways
Rat Community Forum Directory of Rat Laboratories Video Tutorials News RGD Publications RGD Presentations Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources
Advanced Search (OLGA)

GENE - TERM ANNOTATION REPORT

28 Annotations Found.

An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8658410 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast and ovarian cancer
  • Original References(s): PMID:24549055 PMID:25452441 PMID:25503501 PMID:25741868 PMID:26467025 PMID:26534844 PMID:28492532 PMID:30613976 PMID:31159747 PMID:32449991 PMID:33471991 PMID:34426522


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8654580 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:20805886 PMID:25741868 PMID:26467025 PMID:26483394 PMID:26898890 PMID:27621404 PMID:28051113 PMID:28492532


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8660063 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:10047725 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:19383352 PMID:25741868 PMID:28492532


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:13473166 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Breast-ovarian cancer, familial 4
  • Original References(s): PMID:23080121 PMID:23912341 PMID:28492532 PMID:29922827 PMID:32427313 PMID:33479248


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8697764 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:24894818 PMID:25741868 PMID:26580448 PMID:26787654 PMID:28492532 PMID:33471991


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:10767514 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:24093751 PMID:25741868 PMID:28492532 PMID:32566746


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:9851921 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:23912341 PMID:25741868 PMID:28492532 PMID:32566746


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8660062 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:20052722 PMID:25741868 PMID:26467025 PMID:28492532 PMID:32039725


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:11090284 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:16199547 PMID:23080121 PMID:23912341 PMID:25741868 PMID:28492532 PMID:33134171


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:13492370 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32959997


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:9853079 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:17576681 PMID:24894818 PMID:25741868 PMID:26898890 PMID:28492532 PMID:9536098 PMID:9845372


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8698121 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:28873162 PMID:33471991


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 2 | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:13482523|RGD:25324041 (Homo sapiens) & RGD:13482523|RGD:25324041 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:32566746


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:8697801|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:8697801|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:8697801|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:8697801|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:8697801|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:8697801|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:8697801|RGD:9834444 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:13487731|RGD:25329811|RGD:26888439|RGD:26888445 (Homo sapiens) & RGD:13487731|RGD:25329811|RGD:26888439|RGD:26888445 (Homo sapiens) & RGD:13487731|RGD:25329811|RGD:26888439|RGD:26888445 (Homo sapiens) & RGD:13487731|RGD:25329811|RGD:26888439|RGD:26888445 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 1 | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:32566746


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:11092838|RGD:26893353|RGD:8696388|RGD:8697154 (Homo sapiens) & RGD:11092838|RGD:26893353|RGD:8696388|RGD:8697154 (Homo sapiens) & RGD:11092838|RGD:26893353|RGD:8696388|RGD:8697154 (Homo sapiens) & RGD:11092838|RGD:26893353|RGD:8696388|RGD:8697154 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 1 | ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 2 | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8697801 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Breast and/or ovarian cancer
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:33326660 PMID:33471991 PMID:35534704


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:8658397|RGD:8658402|RGD:8696458|RGD:8696557|RGD:9834444 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast and ovarian cancer | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens) & RGD:11049899|RGD:11550646|RGD:150414062|RGD:150423660|RGD:150433170|RGD:150447571|RGD:150468705|RGD:150479909|RGD:150486713|RGD:150502324|RGD:152058137|RGD:152058143|RGD:152058149|RGD:152058165|RGD:152058177|RGD:152058183|RGD:152058192|RGD:25325073 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 2 | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:11091413 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast and ovarian cancer
  • Original References(s): PMID:21227757 PMID:25741868 PMID:28492532 PMID:29348823


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:10768065|RGD:11092838|RGD:8658397|RGD:8658402|RGD:8696458|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:11092838|RGD:8658397|RGD:8658402|RGD:8696458|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:11092838|RGD:8658397|RGD:8658402|RGD:8696458|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:11092838|RGD:8658397|RGD:8658402|RGD:8696458|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:11092838|RGD:8658397|RGD:8658402|RGD:8696458|RGD:9834444 (Homo sapiens) & RGD:10768065|RGD:11092838|RGD:8658397|RGD:8658402|RGD:8696458|RGD:9834444 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast and ovarian cancer | ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:26893353|RGD:8696388|RGD:8697154 (Homo sapiens) & RGD:26893353|RGD:8696388|RGD:8697154 (Homo sapiens) & RGD:26893353|RGD:8696388|RGD:8697154 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8698086 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Breast-ovarian cancer, familial, susceptibility to, 2
  • Original References(s): PMID:11196167 PMID:25741868 PMID:26467025 PMID:28492532 PMID:30982232 PMID:32566746


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8696564 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:11371508 PMID:23080121 PMID:23912341 PMID:24763289 PMID:25503501 PMID:25741868 PMID:26467025 PMID:27153395 PMID:28492532 PMID:28559769 PMID:29478780 PMID:32521533 PMID:33426167 PMID:33479248 PMID:37808486


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8698122 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:26787654 PMID:28492532 PMID:32566746 PMID:33471991 PMID:36091175


    • An association has been curated linking MRE11 and hereditary breast ovarian cancer syndrome 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:8696557 (Homo sapiens)
  • 408 RGD objects have been annotated to hereditary breast ovarian cancer syndrome  (DOID:5683)
  • 21 papers in RGD have been used to annotate MRE11
  • Curation Notes: ClinVar Annotator: match by term: Hereditary breast ovarian cancer syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:33471991


    • Go Back to source page   Continue to Ontology report