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GENE - TERM ANNOTATION REPORT

22 Annotations Found.

An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:8558315 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:11163249


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:10042025 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:22246673


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:8606906 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: CLDN14-related condition
  • Original References(s): PMID:23590985 PMID:24033266 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:28901503 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:23991001 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:8606910 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:24033266 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:11163249 PMID:15880785 PMID:22246673 PMID:25741868 PMID:30303587


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:9689747 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:15880785 PMID:23590985 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:8596597 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:15880785 PMID:25741868 PMID:28492532 PMID:33105617


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:11095655 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:23991001 PMID:24033266 PMID:25741868 PMID:26969326 PMID:27838790 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:25741868 PMID:28492532 PMID:30311386


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:11641927 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:25741868 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:10051658|RGD:11095624 (Homo sapiens) & RGD:10051658|RGD:11095624 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: CLDN14-related condition
  • Original References(s): PMID:24033266


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: CLDN14-related condition
  • Original References(s): PMID:22246673 PMID:23235333 PMID:25741868 PMID:28492532 PMID:30311386


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:10042024 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: CLDN14-related condition
  • Original References(s): PMID:22246673 PMID:25741868


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:9691503 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:15880785 PMID:24033266 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:8606904|RGD:8606908 (Homo sapiens) & RGD:8606904|RGD:8606908 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:8606905|RGD:8606909 (Homo sapiens) & RGD:8606905|RGD:8606909 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:8606907 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:23590985 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:11614400|RGD:11628511|RGD:11630523|RGD:11630760|RGD:11631230|RGD:150547589|RGD:152153477|RGD:405706415 (Homo sapiens) & RGD:11614400|RGD:11628511|RGD:11630523|RGD:11630760|RGD:11631230|RGD:150547589|RGD:152153477|RGD:405706415 (Homo sapiens) & RGD:11614400|RGD:11628511|RGD:11630523|RGD:11630760|RGD:11631230|RGD:150547589|RGD:152153477|RGD:405706415 (Homo sapiens) & RGD:11614400|RGD:11628511|RGD:11630523|RGD:11630760|RGD:11631230|RGD:150547589|RGD:152153477|RGD:405706415 (Homo sapiens) & RGD:11614400|RGD:11628511|RGD:11630523|RGD:11630760|RGD:11631230|RGD:150547589|RGD:152153477|RGD:405706415 (Homo sapiens) & RGD:11614400|RGD:11628511|RGD:11630523|RGD:11630760|RGD:11631230|RGD:150547589|RGD:152153477|RGD:405706415 (Homo sapiens) & RGD:11614400|RGD:11628511|RGD:11630523|RGD:11630760|RGD:11631230|RGD:150547589|RGD:152153477|RGD:405706415 (Homo sapiens) & RGD:11614400|RGD:11628511|RGD:11630523|RGD:11630760|RGD:11631230|RGD:150547589|RGD:152153477|RGD:405706415 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:25741868


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens) & RGD:11621539|RGD:11622638|RGD:11623857|RGD:11623887|RGD:11626372|RGD:11626621|RGD:11629102|RGD:11629254|RGD:11629565|RGD:11646807|RGD:11651169|RGD:11655215|RGD:11655674|RGD:11657738|RGD:11659337|RGD:11662537|RGD:11663278|RGD:11663743|RGD:13838632|RGD:28882419|RGD:28882426|RGD:28882429|RGD:28888296|RGD:28888299|RGD:28888304|RGD:28888308|RGD:28889629|RGD:28896762|RGD:28897107|RGD:28897109|RGD:28897112|RGD:28897114|RGD:28901500|RGD:28901507|RGD:41405871 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:11626464|RGD:11626517|RGD:11639218|RGD:28889625|RGD:8621478 (Homo sapiens) & RGD:11626464|RGD:11626517|RGD:11639218|RGD:28889625|RGD:8621478 (Homo sapiens) & RGD:11626464|RGD:11626517|RGD:11639218|RGD:28889625|RGD:8621478 (Homo sapiens) & RGD:11626464|RGD:11626517|RGD:11639218|RGD:28889625|RGD:8621478 (Homo sapiens) & RGD:11626464|RGD:11626517|RGD:11639218|RGD:28889625|RGD:8621478 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: CLDN14-related condition | ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:28492532


    • An association has been curated linking CLDN14-AS1 and autosomal recessive nonsyndromic deafness 29 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:597721021|RGD:597724698|RGD:597724811|RGD:597724879 (Homo sapiens) & RGD:597721021|RGD:597724698|RGD:597724811|RGD:597724879 (Homo sapiens) & RGD:597721021|RGD:597724698|RGD:597724811|RGD:597724879 (Homo sapiens) & RGD:597721021|RGD:597724698|RGD:597724811|RGD:597724879 (Homo sapiens)
  • 2 RGD objects have been annotated to autosomal recessive nonsyndromic deafness 29  (DOID:0110487)
  • 0 papers in RGD have been used to annotate CLDN14-AS1
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive 29
  • Original References(s): PMID:30311386


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