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GENE - TERM ANNOTATION REPORT

17 Annotations Found.

An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by OMIM:608931
  • Original References(s): PMID:8957026


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by OMIM:608931
  • Original References(s): PMID:11030414


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by OMIM:608931
  • Original References(s): PMID:16087917


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by OMIM:608931
  • Original References(s): PMID:10211467


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by OMIM:608931
  • Original References(s): PMID:16550914 PMID:24033266


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:25741868


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:11030414 PMID:16087917 PMID:28492532 PMID:9443457


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by OMIM:608931


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:28492532 PMID:9158150


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:25741868 PMID:28492532 PMID:9158150


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:10496269 PMID:10514102 PMID:10534268 PMID:15322984 PMID:15367858 PMID:25326635 PMID:25741868 PMID:26467025 PMID:27634344 PMID:28492532 PMID:9097970 PMID:9668239


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:26467025 PMID:8755487 PMID:9158150


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:12417530 PMID:17878953 PMID:19544078 PMID:21940170 PMID:24033266 PMID:24295813 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:15951177 PMID:19064877 PMID:21175599 PMID:25741868 PMID:28024842 PMID:28492532 PMID:29054425 PMID:8957026


    • An association has been curated linking Chrne and congenital myasthenic syndrome 4C 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 CHRNE (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 7 RGD objects have been annotated to congenital myasthenic syndrome 4C  (DOID:0110679)
  • 15 papers in RGD have been used to annotate Chrne
  • Curation Notes: ClinVar Annotator: match by term: Myasthenic syndrome, congenital, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:25741868 PMID:28492532 PMID:8755487


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