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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking Cabp2 and autosomal recessive nonsyndromic deafness in Chinchilla lanigera.        

  • 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 CABP2 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 122 RGD objects have been annotated to autosomal recessive nonsyndromic deafness  (DOID:0050565)
  • 2 papers in RGD have been used to annotate Cabp2
  • Curation Notes: ClinVar Annotator: match by term: Deafness, autosomal recessive
  • Original References(s): PMID:17576681 PMID:22981119 PMID:25741868 PMID:28492532 PMID:30303587 PMID:9536098


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