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GENE - TERM ANNOTATION REPORT

13 Annotations Found.

An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from OMIM Disease Annotation Pipeline
  • The annotation has been inferred from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:25741868


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Dandy-Walker cyst with renal-hepatic-pancreatic dysplasia
  • Original References(s): PMID:18371931, PMID:20007846, PMID:23559409, PMID:25741868, PMID:26673778, PMID:27894351, PMID:28492532, PMID:30311386


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:28492532


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:23188109, PMID:25741868, PMID:28492532


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:17855640, PMID:25741868, PMID:28492532


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • 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 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:18371931, PMID:28492532


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • 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 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:12872122, PMID:25741868, PMID:28492532


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:26184788, PMID:28492532


  • An association has been curated linking Nphp3 and Meckel syndrome 7 in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • 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 from sequence orthology with NPHP3 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 CRRD objects have been annotated to Meckel syndrome 7  (DOID:0070121)
  • 8 papers in CRRD have been used to annotate Nphp3
  • Curation Notes: ClinVar Annotator: match by term: Meckel syndrome type 7
  • Original References(s): PMID:12872122, PMID:28492532


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.