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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Kmt2a and Neurodevelopmental Disorders in Mus musculus.        

  • 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 KMT2A (Homo sapiens) [(EXP) inferred from experiment]
  • 6891 RGD objects have been annotated to Neurodevelopmental Disorders  (DOID:9004429)
  • 23 papers in RGD have been used to annotate Kmt2a
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:28191889


    • An association has been curated linking Kmt2a and Neurodevelopmental Disorders in Mus musculus.        

  • 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 KMT2A (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 6891 RGD objects have been annotated to Neurodevelopmental Disorders  (DOID:9004429)
  • 23 papers in RGD have been used to annotate Kmt2a
  • Curation Notes: ClinVar Annotator: match by term: Neurodevelopmental disorder
  • Original References(s): PMID:22795537 PMID:25574841 PMID:25741868 PMID:25810209 PMID:28120103 PMID:28492532 PMID:29574747 PMID:31157197 PMID:31337854


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