Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   
Search RGD Grant Resources Citing RGD About Us Contact Us
Genes QTLs Strains Markers Genome Information Ontologies Cell Lines References Download Submit Data
OntoMate (Literature Search) JBrowse (Genome Browser) Variant Visualizer Multi-Ontology Enrichment (MOET) Gene-Ortholog Location Finder (GOLF) InterViewer (Protein-Protein Interactions) PhenoMiner (Quatitative Phenotypes) Gene Annotator OLGA (Gene List Generator) RatMine GViewer (Genome Viewer) Overgo Probe Designer ACP Haplotyper Genome Scanner
Aging & Age-Related Disease Cancer Cardiovascular Disease COVID-19 Developmental Disease Diabetes Hematologic Disease Immune & Inflammatory Disease Liver Disease Neurological Disease Obesity & Metabolic Syndrome Renal Disease Respiratory Disease Sensory Organ Disease
Find Models   new Genetic Models Autism Models PhenoMiner (Quantitative Phenotypes) Expected Ranges (Quantitative Phenotype) PhenoMiner Term Comparison Hybrid Rat Diversity Panel Phenotypes GERRC (Gene Editing Rat Resource Center) 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 Poster Archive Nomenclature Guidelines Resource Links Laboratory Resources Employment Resources

GENE - TERM ANNOTATION REPORT

6 Annotations Found.

An association has been curated linking Slc5a7 and distal hereditary motor neuronopathy type 7A in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with SLC5A7 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 9 RGD objects have been annotated to distal hereditary motor neuronopathy type 7A  (DOID:0111201)
  • 20 papers in RGD have been used to annotate Slc5a7


    • An association has been curated linking Slc5a7 and distal hereditary motor neuronopathy type 7A in Rattus norvegicus.        

  • 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 SLC5A7 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 9 RGD objects have been annotated to distal hereditary motor neuronopathy type 7A  (DOID:0111201)
  • 20 papers in RGD have been used to annotate Slc5a7
  • Curation Notes: ClinVar Annotator: match by OMIM:158580
  • Original References(s): PMID:11294660 PMID:23141292 PMID:7420092


    • An association has been curated linking Slc5a7 and distal hereditary motor neuronopathy type 7A in Rattus norvegicus.        

  • 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 SLC5A7 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 9 RGD objects have been annotated to distal hereditary motor neuronopathy type 7A  (DOID:0111201)
  • 20 papers in RGD have been used to annotate Slc5a7
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type viia
  • Original References(s): PMID:28492532


    • An association has been curated linking Slc5a7 and distal hereditary motor neuronopathy type 7A in Rattus norvegicus.        

  • 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 SLC5A7 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 9 RGD objects have been annotated to distal hereditary motor neuronopathy type 7A  (DOID:0111201)
  • 20 papers in RGD have been used to annotate Slc5a7
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type viia
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking Slc5a7 and distal hereditary motor neuronopathy type 7A in Rattus norvegicus.        

  • 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 SLC5A7 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 9 RGD objects have been annotated to distal hereditary motor neuronopathy type 7A  (DOID:0111201)
  • 20 papers in RGD have been used to annotate Slc5a7
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type viia
  • Original References(s): PMID:27569547 PMID:28492532


    • An association has been curated linking Slc5a7 and distal hereditary motor neuronopathy type 7A in Rattus norvegicus.        

  • 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 SLC5A7 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 9 RGD objects have been annotated to distal hereditary motor neuronopathy type 7A  (DOID:0111201)
  • 20 papers in RGD have been used to annotate Slc5a7
  • Curation Notes: ClinVar Annotator: match by term: Neuronopathy, distal hereditary motor, type viia
  • Original References(s): PMID:25741868


    • Go Back to source page   Continue to Ontology report