Send us a Message



Submit Data |  Help |  Video Tutorials |  News |  Publications |  Download |  REST API |  Citing RGD |  Contact   

GENE - TERM ANNOTATION REPORT

42 Annotations Found.

An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by OMIM:614325


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:25741868 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by OMIM:614325
  • Original References(s): PMID:19896112


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by OMIM:614325
  • Original References(s): PMID:21964664


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by OMIM:614325
  • Original References(s): PMID:25741868


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:26467025 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:23533028 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:23207424 PMID:25661985 PMID:27195815 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:18414213 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:18179900 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:18179900 PMID:25741868 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:18179900 PMID:21288692 PMID:25741868 PMID:26467025 PMID:28289584 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:21288692 PMID:25741868 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:21424692 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:23849776 PMID:25741868 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:2504536 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:21827697 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:25326635 PMID:25741868


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:21681106 PMID:23495017 PMID:23533028 PMID:25614873 PMID:28289584


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:19896112 PMID:21964664 PMID:25149956 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:20848651 PMID:22617343 PMID:23533028 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:22617343 PMID:23472757 PMID:23533028 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:26325558 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:18179900 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:17034946 PMID:21424692 PMID:22504536 PMID:24832020 PMID:25741868


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:18490107 PMID:20468056 PMID:28492532 PMID:29221905


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:22405623 PMID:25741868 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:24832020 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:25661985 PMID:26742492 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:22504536


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:25741868 PMID:26350204 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:20347009


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:18414213 PMID:25741868 PMID:26467025 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:17576681 PMID:28492532 PMID:9536098


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:21288692 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:22617343 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:25408897 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:22405623 PMID:28492532


  • An association has been curated linking Nrxn1 and Pitt-Hopkins-like syndrome 2 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 NRXN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 11 RGD objects have been annotated to Pitt-Hopkins-like syndrome 2  (DOID:0111332)
  • 25 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Pitt-Hopkins-like syndrome 2
  • Original References(s): PMID:25741868 PMID:28166811 PMID:28492532


  • Go Back to source page   Continue to Ontology report