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GENE - TERM ANNOTATION REPORT

5 Annotations Found.

An association has been curated linking CLDN14-AS1 and Hearing Loss 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:8596596 (Homo sapiens)
  • 1736 RGD objects have been annotated to Hearing Loss  (DOID:9004538)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive
  • Original References(s): PMID:11163249 PMID:15880785 PMID:22246673 PMID:25741868 PMID:30303587


    • An association has been curated linking CLDN14-AS1 and Hearing Loss 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:126910812 (Homo sapiens)
  • 1736 RGD objects have been annotated to Hearing Loss  (DOID:9004538)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Hearing impairment
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30311386


    • An association has been curated linking CLDN14-AS1 and Hearing Loss 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:10042023 (Homo sapiens)
  • 1736 RGD objects have been annotated to Hearing Loss  (DOID:9004538)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Hearing impairment
  • Original References(s): PMID:22246673 PMID:23235333 PMID:25741868 PMID:28492532 PMID:30311386


    • An association has been curated linking CLDN14-AS1 and Hearing Loss 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:126910636 (Homo sapiens)
  • 1736 RGD objects have been annotated to Hearing Loss  (DOID:9004538)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Hearing impairment
  • Original References(s): PMID:22246673 PMID:23235333 PMID:28492532 PMID:30311386


    • An association has been curated linking CLDN14-AS1 and Hearing Loss 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:126910388|RGD:407572893 (Homo sapiens) & RGD:126910388|RGD:407572893 (Homo sapiens)
  • 1736 RGD objects have been annotated to Hearing Loss  (DOID:9004538)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Hearing impairment | ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive
  • Original References(s): PMID:30311386


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