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GENE - TERM ANNOTATION REPORT

2 Annotations Found.

An association has been curated linking JAM3 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:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens) & RGD:155905606|RGD:155929665|RGD:155962408|RGD:155964861|RGD:156149667|RGD:156168271|RGD:156179273|RGD:156260704|RGD:156272026|RGD:156295440|RGD:156316331|RGD:329378808|RGD:329392379|RGD:401717812|RGD:401720114|RGD:401761145|RGD:401768014|RGD:401857323 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 10 papers in RGD have been used to annotate JAM3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases


    • An association has been curated linking JAM3 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:151792504|RGD:151833097|RGD:155950926|RGD:155998821|RGD:156220751|RGD:156409304 (Homo sapiens) & RGD:151792504|RGD:151833097|RGD:155950926|RGD:155998821|RGD:156220751|RGD:156409304 (Homo sapiens) & RGD:151792504|RGD:151833097|RGD:155950926|RGD:155998821|RGD:156220751|RGD:156409304 (Homo sapiens) & RGD:151792504|RGD:151833097|RGD:155950926|RGD:155998821|RGD:156220751|RGD:156409304 (Homo sapiens) & RGD:151792504|RGD:151833097|RGD:155950926|RGD:155998821|RGD:156220751|RGD:156409304 (Homo sapiens) & RGD:151792504|RGD:151833097|RGD:155950926|RGD:155998821|RGD:156220751|RGD:156409304 (Homo sapiens)
  • 33187 RGD objects have been annotated to genetic disease  (DOID:630)
  • 10 papers in RGD have been used to annotate JAM3
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:28492532


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