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

6 Annotations Found.

An association has been curated linking MAX and paraganglioma in Pan paniscus.        

  • 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 MAX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 41 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 0 papers in RGD have been used to annotate MAX
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:1459463 PMID:1730412 PMID:17576681 PMID:21685915 PMID:22452945 PMID:23551045 PMID:23666964 PMID:25741868 PMID:26070438 PMID:26269449 PMID:27838885 PMID:27903915 PMID:28152038 PMID:28492532 PMID:7630640 PMID:9536098


    • An association has been curated linking MAX and paraganglioma in Pan paniscus.        

  • 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 MAX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 41 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 0 papers in RGD have been used to annotate MAX
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas | ClinVar Annotator: match by term: Paraganglioma, familial malignant
  • Original References(s): PMID:1459463 PMID:1730412 PMID:17576681 PMID:21685915 PMID:22452945 PMID:23551045 PMID:23666964 PMID:25741868 PMID:26070438 PMID:26269449 PMID:27838885 PMID:27903915 PMID:28152038 PMID:28492532 PMID:28552549 PMID:30455982 PMID:34130653 PMID:34439168 PMID:7630640 PMID:9115440 PMID:9536098


    • An association has been curated linking MAX and paraganglioma in Pan paniscus.        

  • 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 MAX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 41 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 0 papers in RGD have been used to annotate MAX
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas | ClinVar Annotator: match by term: Paraganglioma, familial malignant
  • Original References(s): PMID:1459463 PMID:1730412 PMID:17576681 PMID:21685915 PMID:22452945 PMID:23551045 PMID:23666964 PMID:25741868 PMID:26070438 PMID:26269449 PMID:26467025 PMID:27838885 PMID:27903915 PMID:28152038 PMID:28492532 PMID:28552549 PMID:30455982 PMID:34130653 PMID:34439168 PMID:7630640 PMID:9115440 PMID:9536098


    • An association has been curated linking MAX and paraganglioma in Pan paniscus.        

  • 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 MAX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 41 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 0 papers in RGD have been used to annotate MAX
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas
  • Original References(s): PMID:1459463 PMID:1730412 PMID:17576681 PMID:21685915 PMID:22452945 PMID:23551045 PMID:23666964 PMID:25741868 PMID:26070438 PMID:26269449 PMID:26467025 PMID:27838885 PMID:27903915 PMID:28152038 PMID:28384794 PMID:28492532 PMID:28552549 PMID:29909963 PMID:30455982 PMID:33606809 PMID:34130653 PMID:34439168 PMID:7630640 PMID:9115440 PMID:9536098


    • An association has been curated linking MAX and paraganglioma in Pan paniscus.        

  • 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 MAX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 41 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 0 papers in RGD have been used to annotate MAX
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas | ClinVar Annotator: match by term: Hereditary paragangliomas and pheochromocytomas | ClinVar Annotator: match by term: Paraganglioma, familial malignant
  • Original References(s): PMID:1459463 PMID:16199547 PMID:1730412 PMID:17576681 PMID:21685915 PMID:22452945 PMID:23551045 PMID:23666964 PMID:25741868 PMID:26070438 PMID:26269449 PMID:26467025 PMID:27838885 PMID:27903915 PMID:28152038 PMID:28384794 PMID:28492532 PMID:28552549 PMID:29909963 PMID:30455982 PMID:30877234 PMID:33367756 PMID:33493868 PMID:33606809 PMID:34130653 PMID:34439168 PMID:35441217 PMID:37529773 PMID:38141607 PMID:39279998 PMID:7630640 PMID:9115440 PMID:9536098


    • An association has been curated linking MAX and paraganglioma in Pan paniscus.        

  • 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 MAX (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 41 RGD objects have been annotated to paraganglioma  (DOID:0050773)
  • 0 papers in RGD have been used to annotate MAX
  • Curation Notes: ClinVar Annotator: match by term: Hereditary Paragangliomas and Pheochromocytomas | ClinVar Annotator: match by term: Paraganglioma, familial malignant
  • Original References(s): PMID:1459463 PMID:1730412 PMID:17576681 PMID:21685915 PMID:22452945 PMID:23551045 PMID:23666964 PMID:25741868 PMID:26070438 PMID:26269449 PMID:26467025 PMID:27838885 PMID:27903915 PMID:28152038 PMID:28384794 PMID:28492532 PMID:28552549 PMID:29909963 PMID:30455982 PMID:33606809 PMID:34130653 PMID:34439168 PMID:35441217 PMID:38141607 PMID:39279998 PMID:7630640 PMID:9115440 PMID:9536098


    • Go Back to source page   Continue to Ontology report