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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking GNRHR and genetic disease 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:156316731 (Homo sapiens)
  • 40723 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate GNRHR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


    • An association has been curated linking GNRHR and genetic disease 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:8565375 (Homo sapiens)
  • 40723 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate GNRHR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:10022417 PMID:10690855 PMID:10999776 PMID:11397842 PMID:11397871 PMID:12057744 PMID:12364481 PMID:12574221 PMID:12679486 PMID:15728205 PMID:17235395 PMID:20389088 PMID:20696889 PMID:21292259 PMID:21645587 PMID:21664240 PMID:22745237 PMID:23155690 PMID:23643382 PMID:23650335 PMID:25016926 PMID:25077900 PMID:25741868 PMID:26207952 PMID:26467025 PMID:26792935 PMID:28348023 PMID:28492532 PMID:29182666 PMID:30476149 PMID:33223529 PMID:33968656 PMID:34403359 PMID:36407308 PMID:7557974 PMID:9371856


    • An association has been curated linking GNRHR and genetic disease 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:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens) & RGD:155920692|RGD:155947192|RGD:156141794|RGD:156163327|RGD:28888527|RGD:329375519|RGD:405768928|RGD:405768934|RGD:405768940|RGD:405768955|RGD:407520100|RGD:597680567|RGD:597680572|RGD:597680579|RGD:597680583|RGD:597683653 (Homo sapiens)
  • 40723 RGD objects have been annotated to genetic disease  (DOID:630)
  • 9 papers in RGD have been used to annotate GNRHR
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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