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   new 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

GENE - TERM ANNOTATION REPORT

16 Annotations Found.

An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:8566537 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:18087731


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:8566534 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:16501576 PMID:17462671 PMID:17703939 PMID:17900154 PMID:18087731 PMID:18852347 PMID:19363631 PMID:19444281 PMID:22190368 PMID:22722621 PMID:23047679 PMID:23393617 PMID:23463871 PMID:23665167 PMID:25741868 PMID:26467025 PMID:26551617 PMID:26777436 PMID:28492532 PMID:29525178 PMID:30188356 PMID:32579787 PMID:32951934


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:21070605 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: ANG-related condition
  • Original References(s): PMID:17886298 PMID:18087731 PMID:22190368 PMID:25741868 PMID:26467025 PMID:26551617 PMID:28492532


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:8566535 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:17886298 PMID:22384259 PMID:31432357


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:21074422 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:17703939 PMID:18087731 PMID:22190368 PMID:25741868 PMID:28492532


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:28869049 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:22190368 PMID:28492532


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:8566529 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:16501576 PMID:17886298 PMID:17900154 PMID:19153377 PMID:19363631 PMID:19444281 PMID:19449021 PMID:19488901 PMID:20577002 PMID:22190368 PMID:22292843 PMID:22384259 PMID:22499346 PMID:22522484 PMID:22645277 PMID:23047679 PMID:23155438 PMID:23447461 PMID:23463871 PMID:23665167 PMID:25382069 PMID:25741868 PMID:26255299 PMID:26467025 PMID:28444446 PMID:28492532 PMID:31368019 PMID:32111867


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:11612451 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:22384259 PMID:25382069 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:8566536 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:17886298 PMID:23047679 PMID:25741868 PMID:28492532


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:8566528|RGD:8566530|RGD:8566531|RGD:8566532|RGD:8566533 (Homo sapiens) & RGD:8566528|RGD:8566530|RGD:8566531|RGD:8566532|RGD:8566533 (Homo sapiens) & RGD:8566528|RGD:8566530|RGD:8566531|RGD:8566532|RGD:8566533 (Homo sapiens) & RGD:8566528|RGD:8566530|RGD:8566531|RGD:8566532|RGD:8566533 (Homo sapiens) & RGD:8566528|RGD:8566530|RGD:8566531|RGD:8566532|RGD:8566533 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:16501576


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:151893185 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:21621297 PMID:22190368 PMID:25741868 PMID:28492532


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:11546716|RGD:151731803|RGD:401907259 (Homo sapiens) & RGD:11546716|RGD:151731803|RGD:401907259 (Homo sapiens) & RGD:11546716|RGD:151731803|RGD:401907259 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: ANG-related condition | ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens) & RGD:11601154|RGD:11609008|RGD:11609672|RGD:11613674|RGD:11614025|RGD:11615306|RGD:11617180|RGD:11620656|RGD:11620750|RGD:11620860|RGD:11623357|RGD:11623961|RGD:11625529|RGD:11653313|RGD:11653837|RGD:11657027|RGD:11663800|RGD:28869044|RGD:28869046|RGD:28871833|RGD:28911199|RGD:28911255|RGD:28911256|RGD:28911641 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9


    • An association has been curated linking ANG and amyotrophic lateral sclerosis type 9 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:11609884|RGD:11619959|RGD:28869052|RGD:28871830 (Homo sapiens) & RGD:11609884|RGD:11619959|RGD:28869052|RGD:28871830 (Homo sapiens) & RGD:11609884|RGD:11619959|RGD:28869052|RGD:28871830 (Homo sapiens) & RGD:11609884|RGD:11619959|RGD:28869052|RGD:28871830 (Homo sapiens)
  • 5 RGD objects have been annotated to amyotrophic lateral sclerosis type 9  (DOID:0060200)
  • 42 papers in RGD have been used to annotate ANG
  • Curation Notes: ClinVar Annotator: match by term: Amyotrophic lateral sclerosis type 9
  • Original References(s): PMID:28492532


    • Go Back to source page   Continue to Ontology report