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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking Mylk2 and hypertrophic cardiomyopathy 1 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 MYLK2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 59 RGD objects have been annotated to hypertrophic cardiomyopathy 1  (DOID:0110307)
  • 20 papers in RGD have been used to annotate Mylk2


    • An association has been curated linking Mylk2 and hypertrophic cardiomyopathy 1 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 MYLK2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 59 RGD objects have been annotated to hypertrophic cardiomyopathy 1  (DOID:0110307)
  • 20 papers in RGD have been used to annotate Mylk2
  • Curation Notes: ClinVar Annotator: match by term: Familial hypertrophic cardiomyopathy 1 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy 1 | ClinVar Annotator: match by term: Idiopathic hypertrophic subaortic stenosis
  • Original References(s): PMID:11733062 PMID:17576681 PMID:22995991 PMID:23299917 PMID:23861362 PMID:24033266 PMID:24503780 PMID:25741868 PMID:27532257 PMID:28492532 PMID:28704380 PMID:28798025 PMID:29247119 PMID:29915097 PMID:31333075 PMID:31376648 PMID:31568572 PMID:34426522 PMID:9536098


    • An association has been curated linking Mylk2 and hypertrophic cardiomyopathy 1 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 MYLK2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 59 RGD objects have been annotated to hypertrophic cardiomyopathy 1  (DOID:0110307)
  • 20 papers in RGD have been used to annotate Mylk2
  • Curation Notes: ClinVar Annotator: match by term: Hypertrophic cardiomyopathy 1 | ClinVar Annotator: match by term: Idiopathic hypertrophic subaortic stenosis
  • Original References(s): PMID:11733062 PMID:17576681 PMID:22995991 PMID:23299917 PMID:23861362 PMID:24033266 PMID:24503780 PMID:25741868 PMID:28166811 PMID:28492532 PMID:29247119 PMID:31333075 PMID:31568572 PMID:9536098


    • An association has been curated linking Mylk2 and hypertrophic cardiomyopathy 1 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 MYLK2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 59 RGD objects have been annotated to hypertrophic cardiomyopathy 1  (DOID:0110307)
  • 20 papers in RGD have been used to annotate Mylk2
  • Curation Notes: ClinVar Annotator: match by term: Familial hypertrophic cardiomyopathy 1 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy 1 | ClinVar Annotator: match by term: Hypertrophic cardiomyopathy 19 | ClinVar Annotator: match by term: Idiopathic hypertrophic subaortic stenosis
  • Original References(s): PMID:11733062 PMID:17576681 PMID:22995991 PMID:23299917 PMID:23861362 PMID:24033266 PMID:24503780 PMID:25741868 PMID:27532257 PMID:28492532 PMID:28704380 PMID:28798025 PMID:29247119 PMID:29915097 PMID:31333075 PMID:31568572 PMID:9536098


    • An association has been curated linking Mylk2 and hypertrophic cardiomyopathy 1 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with MYLK2 (Homo sapiens) [(EXP) inferred from experiment]
  • 59 RGD objects have been annotated to hypertrophic cardiomyopathy 1  (DOID:0110307)
  • 20 papers in RGD have been used to annotate Mylk2
  • Curation Notes: CTD Direct Evidence: marker/mechanism


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