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1 Annotations Found.

An association has been curated linking Nrxn1 and genetic disease 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]
  • 13004 RGD objects have been annotated to genetic disease  (DOID:630)
  • 31 papers in RGD have been used to annotate Nrxn1
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:17034946 PMID:17576681 PMID:18179900 PMID:18414213 PMID:18490107 PMID:19896112 PMID:20468056 PMID:21288692 PMID:21424692 PMID:21964664 PMID:22405623 PMID:22504536 PMID:22892527 PMID:23495017 PMID:23533028 PMID:23849776 PMID:24064682 PMID:24832020 PMID:25149956 PMID:25418537 PMID:25533962 PMID:25741868 PMID:26350204 PMID:26467025 PMID:28289584 PMID:28492532 PMID:29221905 PMID:29924869 PMID:30031152 PMID:30564305 PMID:32942984 PMID:33004838 PMID:9536098

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