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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Mthfs and Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination 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 MTHFS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  (DOID:9000512)
  • 7 papers in RGD have been used to annotate Mthfs


    • An association has been curated linking Mthfs and Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination 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 MTHFS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  (DOID:9000512)
  • 7 papers in RGD have been used to annotate Mthfs
  • Curation Notes: ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND HYPOMYELINATION
  • Original References(s): PMID:25741868 PMID:30031689


    • An association has been curated linking Mthfs and Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination 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 MTHFS (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination  (DOID:9000512)
  • 7 papers in RGD have been used to annotate Mthfs
  • Curation Notes: ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH MICROCEPHALY, EPILEPSY, AND HYPOMYELINATION
  • Original References(s): PMID:30031689


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