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GENE - TERM ANNOTATION REPORT

22 Annotations Found.

An association has been curated linking C10orf105 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:11096083 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • 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 C10orf105 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:8608774 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • 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 C10orf105 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:11091706 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking C10orf105 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:9689825 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • 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 C10orf105 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:8608779 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking C10orf105 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:8608796 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:24875298 PMID:25468891 PMID:25741868 PMID:28492532


  • An association has been curated linking C10orf105 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:8608798 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:11138009 PMID:18429043 PMID:20146813 PMID:24033266 PMID:28492532


  • An association has been curated linking C10orf105 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:8608799 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • 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 C10orf105 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:8608793 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking C10orf105 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:8608800 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking C10orf105 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:8608785 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking C10orf105 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:8608792 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:28492532


  • An association has been curated linking C10orf105 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:8608789 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:15660226 PMID:18429043 PMID:21569298 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking C10orf105 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:8608773 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:24033266 PMID:28492532


  • An association has been curated linking C10orf105 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:8608797 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:18429043 PMID:24033266 PMID:28492532


  • An association has been curated linking C10orf105 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:8608787 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Usher syndrome type 1B
  • Original References(s): PMID:24033266 PMID:26467025 PMID:28492532


  • An association has been curated linking C10orf105 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:8608780 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • 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 C10orf105 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:38468966 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • 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 C10orf105 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:8558368 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12075507 PMID:15537665 PMID:18273900 PMID:21228398 PMID:24033266 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking C10orf105 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:40904679 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • 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 C10orf105 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:10051820 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • 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 C10orf105 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:8558364 (Homo sapiens)
  • 8 RGD objects have been annotated to Usher Syndrome Type 1B  (DOID:9003365)
  • 1 papers in RGD have been used to annotate C10orf105
  • Curation Notes: ClinVar Annotator: match by term: Retinitis pigmentosa and congenital deafness
  • Original References(s): PMID:12522556 PMID:19683999 PMID:25741868 PMID:28492532 PMID:35020051


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