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GENE - TERM ANNOTATION REPORT

24 Annotations Found.

An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:126743009 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29663639


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:8621290 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:20371544


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:8560403 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:15496425


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:8602151 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:19949040


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:11549050 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:15184594 PMID:25741868 PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:11642896 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:25262156 PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:8660074 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:8572568 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:20371544 PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:26915781 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30719842


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:8597816 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:15496425 PMID:23326516 PMID:24122059 PMID:25741868 PMID:28492532 PMID:30429133


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:10449601 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:25741868 PMID:25900532 PMID:28492532 PMID:32253145


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 in Homo sapiens.        

  • The association was inferred from sequence or structural similarity (ISS)
    		•  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Musk (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: OMIM:616325


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:11642896 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:25262156 PMID:25741868 PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:13625258 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:9536098


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens) & RGD:10052161|RGD:10052162|RGD:11543997|RGD:11545313|RGD:11546313|RGD:11550741|RGD:11552107|RGD:11598715|RGD:11599385|RGD:11603088|RGD:11603882|RGD:11605593|RGD:11606982|RGD:11607306|RGD:11609045|RGD:11610808|RGD:127319012|RGD:127322927|RGD:13211857|RGD:13465829|RGD:13473202|RGD:13495698|RGD:14702242|RGD:14704025|RGD:15110282|RGD:151735777|RGD:15187220|RGD:8660073 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9 | ClinVar Annotator: match by term: Myasthenic syndrome, congenital, 9, associated with acetylcholine receptor deficiency
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:10048727|RGD:13625265|RGD:15134196|RGD:8660072 (Homo sapiens) & RGD:10048727|RGD:13625265|RGD:15134196|RGD:8660072 (Homo sapiens) & RGD:10048727|RGD:13625265|RGD:15134196|RGD:8660072 (Homo sapiens) & RGD:10048727|RGD:13625265|RGD:15134196|RGD:8660072 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens) & RGD:10053442|RGD:11580164|RGD:11580874|RGD:11598899|RGD:11599711|RGD:11601346|RGD:11608041|RGD:11610082|RGD:11612103|RGD:11659616|RGD:13476556|RGD:13479884|RGD:13491536|RGD:13625263|RGD:14728279|RGD:15136732|RGD:26915386|RGD:28877304|RGD:28877550|RGD:28879058|RGD:28879065|RGD:28884723|RGD:28884727|RGD:28887431|RGD:28887439|RGD:28887441|RGD:28887691|RGD:8660071 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:401855023 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29704306


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:10403802 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:16199547 PMID:25612909 PMID:25695962 PMID:25741868 PMID:25900532 PMID:28492532 PMID:8653786


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:8660070|RGD:8660075|RGD:8660076|RGD:8660077 (Homo sapiens) & RGD:8660070|RGD:8660075|RGD:8660076|RGD:8660077 (Homo sapiens) & RGD:8660070|RGD:8660075|RGD:8660076|RGD:8660077 (Homo sapiens) & RGD:8660070|RGD:8660075|RGD:8660076|RGD:8660077 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:11608633|RGD:11610291 (Homo sapiens) & RGD:11608633|RGD:11610291 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:26467025 PMID:28492532


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:11548812|RGD:11552339 (Homo sapiens) & RGD:11548812|RGD:11552339 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9
  • Original References(s): PMID:25741868


    • An association has been curated linking MUSK and congenital myasthenic syndrome 9 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:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens) & RGD:10449604|RGD:11600175|RGD:11609797|RGD:11610677|RGD:11664741|RGD:155266044|RGD:155266045|RGD:155266047|RGD:28877090|RGD:28877307|RGD:28879062|RGD:28887435|RGD:28887684|RGD:28887694 (Homo sapiens)
  • 1 RGD objects have been annotated to congenital myasthenic syndrome 9  (DOID:0110670)
  • 10 papers in RGD have been used to annotate MUSK
  • Curation Notes: ClinVar Annotator: match by term: Congenital myasthenic syndrome 9


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