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GENE - TERM ANNOTATION REPORT

4 Annotations Found.

An association has been curated linking PJVK 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:11666951 (Homo sapiens)
  • 1134 RGD objects have been annotated to Hearing Loss  (DOID:9004538)
  • 4 papers in RGD have been used to annotate PJVK
  • Curation Notes: ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive
  • Original References(s): PMID:28492532


    • An association has been curated linking PJVK 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:11666566 (Homo sapiens)
  • 1134 RGD objects have been annotated to Hearing Loss  (DOID:9004538)
  • 4 papers in RGD have been used to annotate PJVK
  • Curation Notes: ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive
  • Original References(s): PMID:24033266 PMID:28492532


    • An association has been curated linking PJVK 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:11587280|RGD:11588279|RGD:11593758|RGD:11665299 (Homo sapiens) & RGD:11587280|RGD:11588279|RGD:11593758|RGD:11665299 (Homo sapiens) & RGD:11587280|RGD:11588279|RGD:11593758|RGD:11665299 (Homo sapiens) & RGD:11587280|RGD:11588279|RGD:11593758|RGD:11665299 (Homo sapiens)
  • 1134 RGD objects have been annotated to Hearing Loss  (DOID:9004538)
  • 4 papers in RGD have been used to annotate PJVK
  • Curation Notes: ClinVar Annotator: match by term: Nonsyndromic Hearing Loss, Recessive


    • An association has been curated linking PJVK 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:126910657|RGD:126910690 (Homo sapiens) & RGD:126910657|RGD:126910690 (Homo sapiens)
  • 1134 RGD objects have been annotated to Hearing Loss  (DOID:9004538)
  • 4 papers in RGD have been used to annotate PJVK
  • Curation Notes: ClinVar Annotator: match by term: Hearing impairment
  • Original References(s): PMID:30311386


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