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

10 Annotations Found.

An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 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:11558215 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 20
  • Original References(s): PMID:25741868 PMID:27569547


    • An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7


    • An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 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:150452241 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 20
  • Original References(s): PMID:25741868


    • An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 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:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens) & RGD:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens) & RGD:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens) & RGD:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens) & RGD:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens) & RGD:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens) & RGD:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens) & RGD:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens) & RGD:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens) & RGD:13501951|RGD:13607906|RGD:13607911|RGD:15112076|RGD:15113544|RGD:15117402|RGD:15122137|RGD:15131038|RGD:152071219|RGD:38478330 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 20 | ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 20, presynaptic
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 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:11558214 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 20
  • Original References(s): PMID:27569547 PMID:28492532


    • An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 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:11558217 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 20
  • Original References(s): PMID:25741868 PMID:27569547 PMID:28492532


    • An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 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:153349310 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 20
  • Original References(s): PMID:28492532


    • An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 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:156187012 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 20
  • Original References(s): PMID:25741868 PMID:28492532 PMID:33250374 PMID:36703223


    • An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 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:11558216|RGD:11558218 (Homo sapiens) & RGD:11558216|RGD:11558218 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 20
  • Original References(s): PMID:27569547


    • An association has been curated linking SLC5A7 and congenital myasthenic syndrome 20 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:401963653|RGD:401963655|RGD:401964621|RGD:401964622 (Homo sapiens) & RGD:401963653|RGD:401963655|RGD:401964621|RGD:401964622 (Homo sapiens) & RGD:401963653|RGD:401963655|RGD:401964621|RGD:401964622 (Homo sapiens) & RGD:401963653|RGD:401963655|RGD:401964621|RGD:401964622 (Homo sapiens)
  • 2 RGD objects have been annotated to congenital myasthenic syndrome 20  (DOID:0110661)
  • 10 papers in RGD have been used to annotate SLC5A7
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 20


    • Go Back to source page   Continue to Ontology report