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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking LOC102167410 and Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination in Sus scrofa.        

  • 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)
  • 0 papers in RGD have been used to annotate LOC102167410


    • An association has been curated linking LOC102167410 and Neurodevelopmental Disorder with Microcephaly, Epilepsy, and Hypomyelination in Sus scrofa.        

  • 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)
  • 0 papers in RGD have been used to annotate LOC102167410
  • Curation Notes: ClinVar Annotator: match by term: MTHFS-related condition | ClinVar Annotator: match by term: Neurodevelopmental disorder with microcephaly, epilepsy, and hypomyelination
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30031689


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