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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking LOC122094844 and Leptin Receptor Deficiency 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:151356392 (Homo sapiens)
  • 3 RGD objects have been annotated to Leptin Receptor Deficiency  (DOID:9004946)
  • 0 papers in RGD have been used to annotate LOC122094844
  • Curation Notes: ClinVar Annotator: match by term: LEPR-related condition
  • Original References(s): PMID:25741868


    • An association has been curated linking LOC122094844 and Leptin Receptor Deficiency 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:21066744 (Homo sapiens)
  • 3 RGD objects have been annotated to Leptin Receptor Deficiency  (DOID:9004946)
  • 0 papers in RGD have been used to annotate LOC122094844
  • Curation Notes: ClinVar Annotator: match by term: LEPR-related condition
  • Original References(s): PMID:26467025


    • An association has been curated linking LOC122094844 and Leptin Receptor Deficiency 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:28891341 (Homo sapiens)
  • 3 RGD objects have been annotated to Leptin Receptor Deficiency  (DOID:9004946)
  • 0 papers in RGD have been used to annotate LOC122094844
  • Curation Notes: ClinVar Annotator: match by term: LEPR-related condition
  • Original References(s): PMID:28492532


    • An association has been curated linking LOC122094844 and Leptin Receptor Deficiency 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:11578011|RGD:156265136|RGD:28886154|RGD:28891344|RGD:407574422 (Homo sapiens) & RGD:11578011|RGD:156265136|RGD:28886154|RGD:28891344|RGD:407574422 (Homo sapiens) & RGD:11578011|RGD:156265136|RGD:28886154|RGD:28891344|RGD:407574422 (Homo sapiens) & RGD:11578011|RGD:156265136|RGD:28886154|RGD:28891344|RGD:407574422 (Homo sapiens) & RGD:11578011|RGD:156265136|RGD:28886154|RGD:28891344|RGD:407574422 (Homo sapiens)
  • 3 RGD objects have been annotated to Leptin Receptor Deficiency  (DOID:9004946)
  • 0 papers in RGD have been used to annotate LOC122094844
  • Curation Notes: ClinVar Annotator: match by term: LEPR-related condition | ClinVar Annotator: match by term: Leptin receptor deficiency


    • An association has been curated linking LOC122094844 and Leptin Receptor Deficiency 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:12848582 (Homo sapiens)
  • 3 RGD objects have been annotated to Leptin Receptor Deficiency  (DOID:9004946)
  • 0 papers in RGD have been used to annotate LOC122094844
  • Curation Notes: ClinVar Annotator: match by term: Leptin receptor deficiency
  • Original References(s): PMID:21393862 PMID:23760429 PMID:25741868 PMID:26467025 PMID:28492532 PMID:31237021 PMID:33660144 PMID:34097736


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