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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking CRTC1 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:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens) & RGD:155910555|RGD:155916181|RGD:155998571|RGD:156054938|RGD:156055949|RGD:156131167|RGD:156131495|RGD:156193359|RGD:156239190|RGD:156270965|RGD:156365503|RGD:156402367|RGD:329379673|RGD:401734615|RGD:401873351|RGD:401887322|RGD:401898152 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 3 papers in RGD have been used to annotate CRTC1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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