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GENE - TERM ANNOTATION REPORT

7 Annotations Found.

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

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8555900 (Homo sapiens)
  • 1 RGD objects have been annotated to chromosome 17q11.2 deletion syndrome  (DOID:0060403)
  • 0 papers in RGD have been used to annotate Rnf135
  • Curation Notes: ClinVar Annotator: match by term: Macrocephaly, macrosomia, facial dysmorphism syndrome
  • Original References(s): PMID:17632510 PMID:30665703


  • An association has been curated linking Rnf135 and chromosome 17q11.2 deletion syndrome in Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:13784172 (Homo sapiens)
  • 1 RGD objects have been annotated to chromosome 17q11.2 deletion syndrome  (DOID:0060403)
  • 0 papers in RGD have been used to annotate Rnf135
  • Curation Notes: ClinVar Annotator: match by term: Macrocephaly, macrosomia, facial dysmorphism syndrome
  • Original References(s): PMID:17632510 PMID:21681106


  • An association has been curated linking Rnf135 and chromosome 17q11.2 deletion syndrome in Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8555898 (Homo sapiens)
  • 1 RGD objects have been annotated to chromosome 17q11.2 deletion syndrome  (DOID:0060403)
  • 0 papers in RGD have been used to annotate Rnf135
  • Curation Notes: ClinVar Annotator: match by term: Macrocephaly, macrosomia, facial dysmorphism syndrome
  • Original References(s): PMID:17632510 PMID:30665703


  • An association has been curated linking Rnf135 and chromosome 17q11.2 deletion syndrome in Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RNF135 (Homo sapiens)
  • 1 RGD objects have been annotated to chromosome 17q11.2 deletion syndrome  (DOID:0060403)
  • 0 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 Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8555899 (Homo sapiens)
  • 1 RGD objects have been annotated to chromosome 17q11.2 deletion syndrome  (DOID:0060403)
  • 0 papers in RGD have been used to annotate Rnf135
  • Curation Notes: ClinVar Annotator: match by term: Macrocephaly, macrosomia, facial dysmorphism syndrome
  • Original References(s): PMID:17632510 PMID:30665703 PMID:30763456


  • An association has been curated linking Rnf135 and chromosome 17q11.2 deletion syndrome in Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:8555897 (Homo sapiens)
  • 1 RGD objects have been annotated to chromosome 17q11.2 deletion syndrome  (DOID:0060403)
  • 0 papers in RGD have been used to annotate Rnf135
  • Curation Notes: ClinVar Annotator: match by term: Macrocephaly, macrosomia, facial dysmorphism syndrome
  • Original References(s): PMID:17632510 PMID:27535533 PMID:28135719 PMID:30665703


  • An association has been curated linking Rnf135 and chromosome 17q11.2 deletion syndrome in Ictidomys tridecemlineatus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Automated assignment of GO, PW and RDO ISS annotations to Chinchilla, Squirrel, Bonobo and/or Dog genes from Human gene annotations
  • The annotation has been inferred from sequence orthology with RGD:126736966 (Homo sapiens)
  • 1 RGD objects have been annotated to chromosome 17q11.2 deletion syndrome  (DOID:0060403)
  • 0 papers in RGD have been used to annotate Rnf135
  • Curation Notes: ClinVar Annotator: match by term: VAN ASPEREN SYNDROME
  • Original References(s): PMID:25741868


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