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2 Matching Annotations
  1. Last 7 days
  2. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Mutation of the MYL3 gene in a patient with mid-ventricular obstructive hypertrophic cardiomyopathy
    1
    1. ClingenBaseline 24 Oct 2026
      in Baseline Annotations
      Mutation of the MYL3 gene in a patient with mid-ventricular obstructive hypertrophic cardiomyopathy

      PMID: 35288424

      Gene: MLY3

      HGNC ID: 7584

      inferred_gene_hgnc:7584 inferred_gene_source:HGNC_body Cardiomyopathy Annotation
    Visit annotations in context

    Tags

    • inferred_gene_hgnc:7584
    • inferred_gene_source:HGNC_body
    • Cardiomyopathy Annotation

    Annotators

    • ClingenBaseline

    URL

    pmc.ncbi.nlm.nih.gov/articles/PMC8921845/
  3. pmc.ncbi.nlm.nih.gov pmc.ncbi.nlm.nih.gov
    Determining the Pathogenicity of a Genomic Variant of Uncertain Significance Using CRISPR/Cas9 and Human Induced Pluripotent Stem Cells
    1
    1. ClingenBaseline 24 Oct 2026
      in Baseline Annotations
      Determining the Pathogenicity of a Genomic Variant of Uncertain Significance Using CRISPR/Cas9 and Human Induced Pluripotent Stem Cells

      PMID: 29914921

      Gene: MYL3

      HGNC ID: 7584

      inferred_gene_hgnc:7584 inferred_gene_source:HGNC_body Cardiomyopathy Annotation
    Visit annotations in context

    Tags

    • inferred_gene_hgnc:7584
    • inferred_gene_source:HGNC_body
    • Cardiomyopathy Annotation

    Annotators

    • ClingenBaseline

    URL

    pmc.ncbi.nlm.nih.gov/articles/PMC6298866/
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