GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Nus1 and CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1AA 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 NUS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1AA  (DOID:9007792)
  • 4 papers in CRRD have been used to annotate Nus1
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa
  • Original References(s): PMID:25066056

  • This annotation was curated on 2019-06-04 14:22:52.0 by CRRD . For more information contact us

    An association has been curated linking Nus1 and CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1AA 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 NUS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1AA  (DOID:9007792)
  • 4 papers in CRRD have been used to annotate Nus1
  • Curation Notes: ClinVar Annotator: match by term: CONGENITAL DISORDER OF GLYCOSYLATION, TYPE Iaa
  • Original References(s): PMID:28492532

  • This annotation was curated on 2019-06-04 14:26:06.0 by CRRD . For more information contact us

    An association has been curated linking Nus1 and CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1AA 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 NUS1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 1AA  (DOID:9007792)
  • 4 papers in CRRD have been used to annotate Nus1

  • This annotation was curated on 2019-06-05 19:57:04.0 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.