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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Slc33a1 and Congenital Cataracts, Hearing Loss, and Neurodegeneration 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 SLC33A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Congenital Cataracts, Hearing Loss, and Neurodegeneration  (DOID:9005895)
  • 12 papers in RGD have been used to annotate Slc33a1


  • An association has been curated linking Slc33a1 and Congenital Cataracts, Hearing Loss, and Neurodegeneration 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 SLC33A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Congenital Cataracts, Hearing Loss, and Neurodegeneration  (DOID:9005895)
  • 12 papers in RGD have been used to annotate Slc33a1
  • Curation Notes: ClinVar Annotator: match by term: Congenital cataracts, hearing loss, and neurodegeneration
  • Original References(s): PMID:15902551 PMID:22243965 PMID:22508683 PMID:25741868 PMID:28492532 PMID:31194315


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