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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Brat1 and NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES in Ictidomys tridecemlineatus.        

  • 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 BRAT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES  (DOID:9009220)
  • 0 papers in RGD have been used to annotate Brat1


    • An association has been curated linking Brat1 and NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES in Ictidomys tridecemlineatus.        

  • 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 BRAT1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 RGD objects have been annotated to NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES  (DOID:9009220)
  • 0 papers in RGD have been used to annotate Brat1
  • Curation Notes: ClinVar Annotator: match by term: NEURODEVELOPMENTAL DISORDER WITH CEREBELLAR ATROPHY AND WITH OR WITHOUT SEIZURES | ClinVar Annotator: match by term: Neurodevelopmental disorder with cerebellar atrophy and with or without seizures
  • Original References(s): PMID:16452482 PMID:22279524 PMID:25500575 PMID:25741868 PMID:26467025 PMID:26483087 PMID:26494257 PMID:26535877 PMID:26947546 PMID:26964041 PMID:27282546 PMID:27282648 PMID:27480663 PMID:28492532 PMID:28635423 PMID:28752061 PMID:29375859 PMID:29390993 PMID:30552426 PMID:31345272 PMID:32964447 PMID:34747546 PMID:35360849


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