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GENE - TERM ANNOTATION REPORT

48 Annotations Found.

An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by OMIM:257320
  • Original References(s): PMID:10973257 PMID:7682675


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:18414213 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by OMIM:257320
  • Original References(s): PMID:10973257


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2 (Norman-Roberts type)
  • Original References(s): PMID:25741868


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2 (Norman-Roberts type)
  • Original References(s): PMID:18414213


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by OMIM:257320


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:14515139 PMID:25741868 PMID:28419454 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:28492532 PMID:30311386


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:25648840 PMID:25741868 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:18414213 PMID:25741868 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Ha S, etal., J Neurosci. 2017 Jan 25;37(4):960-971. doi: 10.1523/JNEUROSCI.1826-16.2016.
  • The annotation has been inferred from sequence orthology with Reln (Mus musculus) [(IMP) inferred from mutant phenotype]
  • 2 additional annotations were made from Ha S, etal., J Neurosci. 2017 Jan 25;37(4):960-971. doi: 10.1523/JNEUROSCI.1826-16.2016.
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:26544041 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:23757202 PMID:25741868 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:24385848 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:14515139 PMID:14593429 PMID:24828792 PMID:25620207 PMID:25741868 PMID:26467025 PMID:28492532 PMID:29358611


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:23287318 PMID:25741868 PMID:26467025 PMID:28492532 PMID:30891068


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:14515139 PMID:14593429 PMID:25741868 PMID:26467025 PMID:28492532 PMID:29358611


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:14515139 PMID:28419454 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:27064498 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:1451539 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:26467025 PMID:26901136 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29358611


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29358611 PMID:30311386


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:29706646


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:25741868 PMID:26467025


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:14515139 PMID:18414213 PMID:20697953 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:25167861 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:25741868 PMID:28492532 PMID:29056246


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:25648840 PMID:25741868 PMID:26302956 PMID:26467025 PMID:28492532 PMID:29358611


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:16311013 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Lissencephaly 2
  • Original References(s): PMID:24467814 PMID:25741868 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:26467025


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:25741868 PMID:26046367 PMID:28492532 PMID:30311386 PMID:31134136


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:14515139 PMID:23757202 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:14515139 PMID:19319887 PMID:23334996 PMID:25741868 PMID:26467025 PMID:28492532 PMID:29706646


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:18414213 PMID:25741868


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:25648840 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:2564880 PMID:25648840 PMID:25741868 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:25741868 PMID:26459092 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:16311013 PMID:19435634 PMID:25741868 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:14515139 PMID:24828792 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Reln and Norman-Roberts syndrome 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 RELN (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 1 RGD objects have been annotated to Norman-Roberts syndrome  (DOID:0060902)
  • 59 papers in RGD have been used to annotate Reln
  • Curation Notes: ClinVar Annotator: match by term: Norman-Roberts syndrome
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532 PMID:28677532 PMID:29969175


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