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GENE - TERM ANNOTATION REPORT

20 Annotations Found.

An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by OMIM:613443


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by OMIM:613443
  • Original References(s): PMID:20513142


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:28492532


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by OMIM:613443
  • Original References(s): PMID:18414213


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by OMIM:613443
  • Original References(s): PMID:24088041 PMID:26633545


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:25741868


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by OMIM:613443
  • Original References(s): PMID:23001426


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:28492532 PMID:29706646


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:18414213 PMID:28492532 PMID:30376817


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:20513142 PMID:28492532


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:28492532 PMID:28554332


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:27748065 PMID:28492532


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:20333642 PMID:22031302 PMID:28492532


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:7679508


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:27255693


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:18414213 PMID:28492532


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:19592390 PMID:19876902 PMID:20513142 PMID:23001426 PMID:25741868 PMID:28492532


  • An association has been curated linking Mef2c and autosomal dominant mental retardation 20 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 MEF2C (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to autosomal dominant mental retardation 20  (DOID:0070050)
  • 20 papers in RGD have been used to annotate Mef2c
  • Curation Notes: ClinVar Annotator: match by term: Mental retardation, stereotypic movements, epilepsy, and/or cerebral malformations
  • Original References(s): PMID:25741869


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