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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking Ndufb11 and Linear Skin Defects with Multiple Congenital Anomalies 3 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 NDUFB11 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Linear Skin Defects with Multiple Congenital Anomalies 3  (DOID:9003152)
  • 3 papers in CRRD have been used to annotate Ndufb11

  • This annotation was curated on 2020-01-15 19:57:11.0 by CRRD . For more information contact us

    An association has been curated linking Ndufb11 and Linear Skin Defects with Multiple Congenital Anomalies 3 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 NDUFB11 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Linear Skin Defects with Multiple Congenital Anomalies 3  (DOID:9003152)
  • 3 papers in CRRD have been used to annotate Ndufb11
  • Curation Notes: ClinVar Annotator: match by term: Linear skin defects with multiple congenital anomalies 3
  • Original References(s): PMID:25741868, PMID:25772934

  • This annotation was curated on 2020-01-14 05:54:30.0 by CRRD . For more information contact us

    An association has been curated linking Ndufb11 and Linear Skin Defects with Multiple Congenital Anomalies 3 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 NDUFB11 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Linear Skin Defects with Multiple Congenital Anomalies 3  (DOID:9003152)
  • 3 papers in CRRD have been used to annotate Ndufb11
  • Curation Notes: ClinVar Annotator: match by term: Linear skin defects with multiple congenital anomalies 3
  • Original References(s): PMID:25772934

  • This annotation was curated on 2020-01-14 05:54:39.0 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.