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GENE - TERM ANNOTATION REPORT

31 Annotations Found.

An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609316 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15537665 PMID:15660226 PMID:24033266


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609345 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:21569298 PMID:22815625 PMID:24033266 PMID:25468891 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609318 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:16679490 PMID:21569298 PMID:22183965 PMID:24033266 PMID:25741868 PMID:26467025 PMID:27861356 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609307 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609381 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:11599403 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25468891 PMID:25741868 PMID:28492532 PMID:30311386


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609374 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:24831256 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:11603688 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:11639605 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:24498627 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609371 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15660226 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609352 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609347 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15660226 PMID:24033266 PMID:25262649 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8558376 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11398101 PMID:11487575 PMID:12711741 PMID:14570705 PMID:15028842 PMID:20301442 PMID:22815625 PMID:24033266 PMID:24105371 PMID:25262649 PMID:25307757 PMID:25525159 PMID:25741868 PMID:27460420 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:11603484 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:28908875 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:11600960 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:17576681 PMID:25741868 PMID:28492532 PMID:30718709 PMID:9536098


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609354 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609306 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609369 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:22135276 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609309 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609311 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:11647181 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:9691059 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23967202 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:28905700 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:23967202 PMID:24164807 PMID:25741868 PMID:28492532 PMID:28847902 PMID:30245029


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8609379 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:8692320 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:15660226 PMID:22135276 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:28905378 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:25741868 PMID:27058588 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:11542110 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:16963483 PMID:24940003 PMID:25741868 PMID:26791358 PMID:27440999 PMID:28492532


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:11089930 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26166082 PMID:28492532 PMID:34416374


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:11095498 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24618850 PMID:25741868


  • An association has been curated linking PCDH15 and Usher Syndrome Type 1B 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:21404168 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 9 papers in RGD have been used to annotate PCDH15
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11398101 PMID:11487575 PMID:14570705 PMID:25741868 PMID:28492532 PMID:33576794


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