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GENE - TERM ANNOTATION REPORT

10 Annotations Found.

An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:11588878 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:28492532


  • An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:11591530 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:28492532


  • An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:8643420 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:17855640 PMID:24033266 PMID:25741868 PMID:28492532


  • An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:11544187 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:9688732 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:11648541 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7


  • An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:10049607 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:38479936 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:11587395 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Dandy-Walker cyst with renal-hepatic-pancreatic dysplasia
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking NPHP3-AS1 and Meckel syndrome 7 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:126735606 (Homo sapiens)
  • 4 RGD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 0 papers in RGD have been used to annotate NPHP3-AS1
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:25741868 PMID:28492532


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