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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking ARCN1 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:401750555 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate ARCN1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868


    • An association has been curated linking ARCN1 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:155940871 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate ARCN1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking ARCN1 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:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens) & RGD:155909520|RGD:156043569|RGD:156059365|RGD:156061267|RGD:156079702|RGD:156123439|RGD:156150044|RGD:156166784|RGD:156240060|RGD:156333790|RGD:156338459|RGD:329401567|RGD:401747358|RGD:401771690|RGD:401867453|RGD:405674081|RGD:405674089|RGD:405674094|RGD:405674098|RGD:407465203|RGD:407512909|RGD:407512967|RGD:407512976 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate ARCN1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking ARCN1 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:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens) & RGD:151721383|RGD:151744537|RGD:151754461|RGD:151844962|RGD:155983424|RGD:156020482|RGD:156420030|RGD:39456723|RGD:39456764|RGD:405216391|RGD:405240220 (Homo sapiens)
  • 27244 RGD objects have been annotated to genetic disease  (DOID:630)
  • 2 papers in RGD have been used to annotate ARCN1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


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