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


1 Annotations Found.

An association has been curated linking Caln1 and Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability 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 CALN1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 4 RGD objects have been annotated to Multiple Congenital Anomalies/Dysmorphic Syndrome-Intellectual Disability  (DOID:9005747)
  • 3 papers in RGD have been used to annotate Caln1
  • Curation Notes: ClinVar Annotator: match by term: Multiple congenital anomalies/dysmorphic syndrome-intellectual disability
  • Original References(s): PMID:23332918

  • Go Back to source page   Continue to Ontology report

    NHLBI Logo

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