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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking NUP107 and ovarian dysgenesis 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:13791386 (Homo sapiens)
  • 1 RGD objects have been annotated to ovarian dysgenesis 6  (DOID:0080498)
  • 4 papers in RGD have been used to annotate NUP107
  • Curation Notes: ClinVar Annotator: match by term: Ovarian dysgenesis 6
  • Original References(s): PMID:26485283


    • An association has been curated linking NUP107 and ovarian dysgenesis 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 1 RGD objects have been annotated to ovarian dysgenesis 6  (DOID:0080498)
  • 4 papers in RGD have been used to annotate NUP107


    • An association has been curated linking NUP107 and ovarian dysgenesis 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:151709570 (Homo sapiens)
  • 1 RGD objects have been annotated to ovarian dysgenesis 6  (DOID:0080498)
  • 4 papers in RGD have been used to annotate NUP107
  • Curation Notes: ClinVar Annotator: match by term: Ovarian dysgenesis 6


    • An association has been curated linking NUP107 and ovarian dysgenesis 6 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • 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 by association of genotype and phenotype with RGD:15190417 (Homo sapiens)
  • 1 RGD objects have been annotated to ovarian dysgenesis 6  (DOID:0080498)
  • 4 papers in RGD have been used to annotate NUP107
  • Curation Notes: ClinVar Annotator: match by term: Ovarian dysgenesis 6
  • Original References(s): PMID:25741868 PMID:28492532


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