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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking KIT and Dysgerminoma 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:8563925 (Homo sapiens)
  • 13 RGD objects have been annotated to Dysgerminoma  (HP:0100621)
  • 51 papers in RGD have been used to annotate KIT
  • Curation Notes: ClinVar Annotator: match by term: Dysgerminoma
  • Original References(s): PMID:10362788 PMID:11276010 PMID:15790786 PMID:16731599 PMID:18955458 PMID:19164557 PMID:20147452 PMID:21642685 PMID:21690468 PMID:25157968 PMID:25741868 PMID:26822237 PMID:7530509 PMID:9438854


    • An association has been curated linking KIT and Dysgerminoma 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:8563914 (Homo sapiens)
  • 13 RGD objects have been annotated to Dysgerminoma  (HP:0100621)
  • 51 papers in RGD have been used to annotate KIT
  • Curation Notes: ClinVar Annotator: match by term: Dysgerminoma
  • Original References(s): PMID:11380399 PMID:11493470 PMID:15972446 PMID:16352739 PMID:16384925 PMID:16731599 PMID:16912224 PMID:17259998 PMID:18024392 PMID:18986703 PMID:19164557 PMID:19262599 PMID:19865100 PMID:21689725 PMID:22504184 PMID:23582185 PMID:23714533 PMID:24045550 PMID:25157968 PMID:25741868 PMID:26158763 PMID:26822237 PMID:27777718 PMID:28492532 PMID:7479840 PMID:7691885 PMID:8589724 PMID:9827716 PMID:9990072


    • An association has been curated linking KIT and Dysgerminoma 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:13435565 (Homo sapiens)
  • 13 RGD objects have been annotated to Dysgerminoma  (HP:0100621)
  • 51 papers in RGD have been used to annotate KIT
  • Curation Notes: ClinVar Annotator: match by term: Dysgerminoma
  • Original References(s): PMID:26822237


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