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GENE - TERM ANNOTATION REPORT

11 Annotations Found.

An association has been curated linking LOC126806422 and myofibrillar myopathy 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:8610145 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myofibrillar, 9, with early respiratory failure
  • Original References(s): PMID:23861362 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:8691542 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, distal, with early respiratory failure, autosomal dominant
  • Original References(s): PMID:23396983 PMID:24033266 PMID:25741868 PMID:26467025 PMID:26516846 PMID:28492532


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:10058122 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, distal, with early respiratory failure, autosomal dominant
  • Original References(s): PMID:25741868


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:8610144 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, distal, with early respiratory failure, autosomal dominant
  • Original References(s): PMID:23861362 PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:8610146 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myofibrillar, 9, with early respiratory failure
  • Original References(s): PMID:10462489 PMID:11717165 PMID:12145747 PMID:12669942 PMID:17444505 PMID:1745277 PMID:18948003 PMID:21617319 PMID:21810661 PMID:22335739 PMID:23418287 PMID:23518707 PMID:24033266 PMID:24105469 PMID:24395473 PMID:24503780 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:8610155 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myofibrillar, 9, with early respiratory failure
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532 PMID:30656044


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:11647135|RGD:28868755|RGD:28869666|RGD:28869895 (Homo sapiens) & RGD:11647135|RGD:28868755|RGD:28869666|RGD:28869895 (Homo sapiens) & RGD:11647135|RGD:28868755|RGD:28869666|RGD:28869895 (Homo sapiens) & RGD:11647135|RGD:28868755|RGD:28869666|RGD:28869895 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myofibrillar, 9, with early respiratory failure


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:8610143|RGD:9688522 (Homo sapiens) & RGD:8610143|RGD:9688522 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Hereditary myopathy with early respiratory failure | ClinVar Annotator: match by term: Myopathy, myofibrillar, 9, with early respiratory failure
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:13470018|RGD:8610152|RGD:8610153|RGD:9689382|RGD:9693614 (Homo sapiens) & RGD:13470018|RGD:8610152|RGD:8610153|RGD:9689382|RGD:9693614 (Homo sapiens) & RGD:13470018|RGD:8610152|RGD:8610153|RGD:9689382|RGD:9693614 (Homo sapiens) & RGD:13470018|RGD:8610152|RGD:8610153|RGD:9689382|RGD:9693614 (Homo sapiens) & RGD:13470018|RGD:8610152|RGD:8610153|RGD:9689382|RGD:9693614 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Hereditary myopathy with early respiratory failure | ClinVar Annotator: match by term: Myopathy, distal, with early respiratory failure, autosomal dominant | ClinVar Annotator: match by term: Myopathy, myofibrillar, 9, with early respiratory failure
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:12840458|RGD:12898039|RGD:13614658 (Homo sapiens) & RGD:12840458|RGD:12898039|RGD:13614658 (Homo sapiens) & RGD:12840458|RGD:12898039|RGD:13614658 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, distal, with early respiratory failure, autosomal dominant | ClinVar Annotator: match by term: Myopathy, myofibrillar, 9, with early respiratory failure
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking LOC126806422 and myofibrillar myopathy 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:8643210|RGD:8643211 (Homo sapiens) & RGD:8643210|RGD:8643211 (Homo sapiens)
  • 22 RGD objects have been annotated to myofibrillar myopathy 9  (DOID:0111188)
  • 0 papers in RGD have been used to annotate LOC126806422
  • Curation Notes: ClinVar Annotator: match by term: Myopathy, myofibrillar, 9, with early respiratory failure
  • Original References(s): PMID:24033266 PMID:28492532


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