Send us a Message



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

GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking KCNAB2 and chromosome 1p36 deletion syndrome in Homo sapiens.        

  • The association was inferred from sequence or structural similarity (ISS)
  •  
  • The annotation was made from RGD automated import pipeline for MGI gene-to-disease annotations
  • The annotation has been inferred from sequence or structural similarity with Kcnab2 (Mus musculus) [(IAGP) inferred by association of genotype and phenotype]
  • 399 RGD objects have been annotated to chromosome 1p36 deletion syndrome  (DOID:0060410)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: OMIM:607872


  • An association has been curated linking KCNAB2 and chromosome 1p36 deletion syndrome in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • 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 by association of genotype and phenotype with RGD:329351260 (Homo sapiens)
  • 399 RGD objects have been annotated to chromosome 1p36 deletion syndrome  (DOID:0060410)
  • 4 papers in RGD have been used to annotate KCNAB2
  • Curation Notes: ClinVar Annotator: match by term: Chromosome 1p36 deletion syndrome


  • Go Back to source page   Continue to Ontology report