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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking SNHG31 and autosomal recessive congenital ichthyosis 4A 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:8557053 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive congenital ichthyosis 4A  (DOID:0060712)
  • 0 papers in RGD have been used to annotate SNHG31
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive congenital ichthyosis 4A
  • Original References(s): PMID:15756637 PMID:25741868 PMID:28492532


    • An association has been curated linking SNHG31 and autosomal recessive congenital ichthyosis 4A 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:8557054 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive congenital ichthyosis 4A  (DOID:0060712)
  • 0 papers in RGD have been used to annotate SNHG31
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive congenital ichthyosis 4A
  • Original References(s): PMID:15756637 PMID:20672373 PMID:25741868 PMID:28492532 PMID:30916489 PMID:32293521


    • An association has been curated linking SNHG31 and autosomal recessive congenital ichthyosis 4A 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:11583507|RGD:14696251|RGD:329954528|RGD:38462765 (Homo sapiens) & RGD:11583507|RGD:14696251|RGD:329954528|RGD:38462765 (Homo sapiens) & RGD:11583507|RGD:14696251|RGD:329954528|RGD:38462765 (Homo sapiens) & RGD:11583507|RGD:14696251|RGD:329954528|RGD:38462765 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive congenital ichthyosis 4A  (DOID:0060712)
  • 0 papers in RGD have been used to annotate SNHG31
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive congenital ichthyosis 4A
  • Original References(s): PMID:25741868


    • An association has been curated linking SNHG31 and autosomal recessive congenital ichthyosis 4A 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:11543375|RGD:11552540 (Homo sapiens) & RGD:11543375|RGD:11552540 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive congenital ichthyosis 4A  (DOID:0060712)
  • 0 papers in RGD have been used to annotate SNHG31
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive congenital ichthyosis 4A
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking SNHG31 and autosomal recessive congenital ichthyosis 4A 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:151729940|RGD:401828325 (Homo sapiens) & RGD:151729940|RGD:401828325 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive congenital ichthyosis 4A  (DOID:0060712)
  • 0 papers in RGD have been used to annotate SNHG31
  • Curation Notes: ClinVar Annotator: match by term: Autosomal recessive congenital ichthyosis 4A


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