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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking SSR4 and congenital disorder of glycosylation Iy in Sus scrofa.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • 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 or structural similarity with Ssr4 (Ictidomys tridecemlineatus)
  • 1 CRRD objects have been annotated to congenital disorder of glycosylation Iy  (DOID:0080574)
  • 0 papers in CRRD have been used to annotate SSR4

  • This annotation was curated on 2019-10-10 22:51:01.0 by CRRD . For more information contact us

    An association has been curated linking SSR4 and congenital disorder of glycosylation Iy in Sus scrofa.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • 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 or structural similarity with Ssr4 (Ictidomys tridecemlineatus)
  • 1 CRRD objects have been annotated to congenital disorder of glycosylation Iy  (DOID:0080574)
  • 0 papers in CRRD have been used to annotate SSR4
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1y
  • Original References(s): PMID:26264460

  • This annotation was curated on 2019-10-10 22:51:01.0 by CRRD . For more information contact us

    An association has been curated linking SSR4 and congenital disorder of glycosylation Iy in Sus scrofa.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • 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 or structural similarity with Ssr4 (Ictidomys tridecemlineatus)
  • 1 CRRD objects have been annotated to congenital disorder of glycosylation Iy  (DOID:0080574)
  • 0 papers in CRRD have been used to annotate SSR4
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1y
  • Original References(s): PMID:24218363

  • This annotation was curated on 2019-10-10 22:51:01.0 by CRRD . For more information contact us

    An association has been curated linking SSR4 and congenital disorder of glycosylation Iy in Sus scrofa.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • 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 or structural similarity with Ssr4 (Ictidomys tridecemlineatus)
  • 1 CRRD objects have been annotated to congenital disorder of glycosylation Iy  (DOID:0080574)
  • 0 papers in CRRD have been used to annotate SSR4
  • Curation Notes: ClinVar Annotator: match by term: Congenital disorder of glycosylation type 1y
  • Original References(s): PMID:25326635, PMID:25741868, PMID:26264460

  • This annotation was curated on 2019-10-10 22:51:01.0 by CRRD . For more information contact us

    An association has been curated linking SSR4 and congenital disorder of glycosylation Iy 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 SSR4 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to congenital disorder of glycosylation Iy  (DOID:0080574)
  • 0 papers in CRRD have been used to annotate SSR4

  • This annotation was curated on 2019-10-09 19:57:07.0 by CRRD . For more information contact us

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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.