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GENE - TERM ANNOTATION REPORT

1 Annotations Found.

An association has been curated linking KIF3B and genetic disease 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:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens) & RGD:155931819|RGD:155937681|RGD:155962602|RGD:156025027|RGD:156112719|RGD:156166718|RGD:156342062|RGD:401731375|RGD:401734542|RGD:401738210|RGD:401753444|RGD:401760811|RGD:401770563|RGD:401783510|RGD:401874752 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 4 papers in RGD have been used to annotate KIF3B
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


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