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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking Rnf135 and chromosome 17q11.2 deletion syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • The annotation has been inferred from sequence orthology with RNF135 (Homo sapiens) [(EXP) inferred from experiment]
  • 1 RGD objects have been annotated to chromosome 17q11.2 deletion syndrome  (DOID:0060403)
  • 6 papers in RGD have been used to annotate Rnf135
  • Curation Notes: CTD Direct Evidence: marker/mechanism
  • Original References(s): PMID:17632510


  • An association has been curated linking Rnf135 and chromosome 17q11.2 deletion syndrome 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 RNF135 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to chromosome 17q11.2 deletion syndrome  (DOID:0060403)
  • 6 papers in RGD have been used to annotate Rnf135
  • Curation Notes: ClinVar Annotator: match by term: Chromosome 17q11.2 deletion syndrome, 1.4Mb | ClinVar Annotator: match by term: Macrocephaly, macrosomia, facial dysmorphism syndrome
  • Original References(s): PMID:17632510 PMID:21681106 PMID:25741868 PMID:27535533 PMID:28135719 PMID:30665703 PMID:30763456


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