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GENE - TERM ANNOTATION REPORT

8 Annotations Found.

An association has been curated linking FOXL2 and primary ovarian insufficiency 3 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:9686551 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 3  (DOID:0080860)
  • 9 papers in RGD have been used to annotate FOXL2
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 3
  • Original References(s): PMID:12529855 PMID:18635577 PMID:19515849 PMID:25741868 PMID:28492532 PMID:31048069 PMID:31077882


    • An association has been curated linking FOXL2 and primary ovarian insufficiency 3 in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • 2 RGD objects have been annotated to primary ovarian insufficiency 3  (DOID:0080860)
  • 9 papers in RGD have been used to annotate FOXL2


    • An association has been curated linking FOXL2 and primary ovarian insufficiency 3 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:155643958 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 3  (DOID:0080860)
  • 9 papers in RGD have been used to annotate FOXL2
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 3
  • Original References(s): PMID:25741868


    • An association has been curated linking FOXL2 and primary ovarian insufficiency 3 in Homo sapiens.        

  • The association was inferred from experiment (EXP)
    		•  
  • The annotation was made from RGD automated import pipeline for CTD gene-to-disease annotations
  • 2 RGD objects have been annotated to primary ovarian insufficiency 3  (DOID:0080860)
  • 9 papers in RGD have been used to annotate FOXL2
  • Curation Notes: CTD Direct Evidence: marker/mechanism


    • An association has been curated linking FOXL2 and primary ovarian insufficiency 3 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:156296793 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 3  (DOID:0080860)
  • 9 papers in RGD have been used to annotate FOXL2
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 3
  • Original References(s): PMID:12149404 PMID:25741868


    • An association has been curated linking FOXL2 and primary ovarian insufficiency 3 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:8596606 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 3  (DOID:0080860)
  • 9 papers in RGD have been used to annotate FOXL2
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 3
  • Original References(s): PMID:12161610 PMID:19429596 PMID:25741868 PMID:28492532


    • An association has been curated linking FOXL2 and primary ovarian insufficiency 3 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:8558324|RGD:8596605 (Homo sapiens) & RGD:8558324|RGD:8596605 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 3  (DOID:0080860)
  • 9 papers in RGD have been used to annotate FOXL2
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 3
  • Original References(s): PMID:12149404


    • An association has been curated linking FOXL2 and primary ovarian insufficiency 3 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:13516891|RGD:13527748 (Homo sapiens) & RGD:13516891|RGD:13527748 (Homo sapiens)
  • 2 RGD objects have been annotated to primary ovarian insufficiency 3  (DOID:0080860)
  • 9 papers in RGD have been used to annotate FOXL2
  • Curation Notes: ClinVar Annotator: match by term: Premature ovarian failure 3
  • Original References(s): PMID:29378385


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