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

8 Annotations Found.

An association has been curated linking CSRNP3 and hereditary sensory and autonomic neuropathy type 2A 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:26891923 (Homo sapiens)
  • 24 RGD objects have been annotated to hereditary sensory and autonomic neuropathy type 2A  (DOID:0070155)
  • 2 papers in RGD have been used to annotate CSRNP3
  • Curation Notes: ClinVar Annotator: match by term: Neuropathy, hereditary sensory and autonomic, type 2A
  • Original References(s): PMID:21416599 PMID:21692795 PMID:23016767 PMID:23184456 PMID:26068938 PMID:28492532


    • An association has been curated linking CSRNP3 and hereditary sensory and autonomic neuropathy type 2A 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:14718400 (Homo sapiens)
  • 24 RGD objects have been annotated to hereditary sensory and autonomic neuropathy type 2A  (DOID:0070155)
  • 2 papers in RGD have been used to annotate CSRNP3
  • Curation Notes: ClinVar Annotator: match by term: Neuropathy, hereditary sensory and autonomic, type 2A
  • Original References(s): PMID:23016767 PMID:28492532


    • An association has been curated linking CSRNP3 and hereditary sensory and autonomic neuropathy type 2A 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:14717636 (Homo sapiens)
  • 24 RGD objects have been annotated to hereditary sensory and autonomic neuropathy type 2A  (DOID:0070155)
  • 2 papers in RGD have been used to annotate CSRNP3
  • Curation Notes: ClinVar Annotator: match by term: Neuropathy, hereditary sensory and autonomic, type 2A
  • Original References(s): PMID:17561957 PMID:18479393 PMID:19400878 PMID:21719429 PMID:25253744 PMID:25524840 PMID:28492532


    • An association has been curated linking CSRNP3 and hereditary sensory and autonomic neuropathy type 2A 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:13620702 (Homo sapiens)
  • 24 RGD objects have been annotated to hereditary sensory and autonomic neuropathy type 2A  (DOID:0070155)
  • 2 papers in RGD have been used to annotate CSRNP3
  • Curation Notes: ClinVar Annotator: match by term: Neuropathy, hereditary sensory and autonomic, type 2A
  • Original References(s): PMID:17470132 PMID:17561957 PMID:18479393 PMID:19400878 PMID:21719429 PMID:25439579 PMID:25524840 PMID:25995458 PMID:28492532


    • An association has been curated linking CSRNP3 and hereditary sensory and autonomic neuropathy type 2A 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:126920471 (Homo sapiens)
  • 24 RGD objects have been annotated to hereditary sensory and autonomic neuropathy type 2A  (DOID:0070155)
  • 2 papers in RGD have been used to annotate CSRNP3
  • Curation Notes: ClinVar Annotator: match by term: Neuropathy, hereditary sensory and autonomic, type 2A
  • Original References(s): PMID:15133511 PMID:16865694 PMID:17347258 PMID:17470132 PMID:17561957 PMID:18327258 PMID:18930999 PMID:19304393 PMID:19400878 PMID:20358599 PMID:20522430 PMID:21068128 PMID:21258341 PMID:21719429 PMID:22495306 PMID:23020937 PMID:23559409 PMID:23662938 PMID:24650168 PMID:24876116 PMID:25492405 PMID:26068938 PMID:27491411 PMID:28492532 PMID:29068549


    • An association has been curated linking CSRNP3 and hereditary sensory and autonomic neuropathy type 2A 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:14717341 (Homo sapiens)
  • 24 RGD objects have been annotated to hereditary sensory and autonomic neuropathy type 2A  (DOID:0070155)
  • 2 papers in RGD have been used to annotate CSRNP3
  • Curation Notes: ClinVar Annotator: match by term: Neuropathy, hereditary sensory and autonomic, type 2A
  • Original References(s): PMID:16865694 PMID:17347258 PMID:17470132 PMID:17561957 PMID:18930999 PMID:19304393 PMID:19400878 PMID:20522430 PMID:21719429 PMID:23662938 PMID:26068938 PMID:28379373 PMID:28492532


    • An association has been curated linking CSRNP3 and hereditary sensory and autonomic neuropathy type 2A 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:156438170 (Homo sapiens)
  • 24 RGD objects have been annotated to hereditary sensory and autonomic neuropathy type 2A  (DOID:0070155)
  • 2 papers in RGD have been used to annotate CSRNP3
  • Curation Notes: ClinVar Annotator: match by term: Neuropathy, hereditary sensory and autonomic, type 2A
  • Original References(s): PMID:21692795 PMID:23016767 PMID:28492532


    • An association has been curated linking CSRNP3 and hereditary sensory and autonomic neuropathy type 2A 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:156442816 (Homo sapiens)
  • 24 RGD objects have been annotated to hereditary sensory and autonomic neuropathy type 2A  (DOID:0070155)
  • 2 papers in RGD have been used to annotate CSRNP3
  • Curation Notes: ClinVar Annotator: match by term: Neuropathy, hereditary sensory and autonomic, type 2A
  • Original References(s): PMID:25253744 PMID:28492532


    • Go Back to source page   Continue to Ontology report