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 ABCC8 and genetic disease in Pan paniscus.        

  • 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 ABCC8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 17786 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate ABCC8
  • Curation Notes: ClinVar Annotator: match by term: Hereditary disease | ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:10204114 PMID:10447255 PMID:10487673 PMID:10923633 PMID:11272143 PMID:11999683 PMID:12941782 PMID:14692646 PMID:14715863 PMID:15356046 PMID:15562009 PMID:15579781 PMID:16357843 PMID:16429405 PMID:16860127 PMID:17378627 PMID:18339976 PMID:18414213 PMID:18493152 PMID:20672374 PMID:21716120 PMID:21851374 PMID:23345197 PMID:24401662 PMID:25306193 PMID:25972930 PMID:26467025 PMID:27175728 PMID:27754802 PMID:28492532 PMID:7716548 PMID:8923011 PMID:9618169 PMID:9648840


  • An association has been curated linking ABCC8 and genetic disease in Pan paniscus.        

  • 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 ABCC8 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 17786 RGD objects have been annotated to genetic disease  (DOID:630)
  • 0 papers in RGD have been used to annotate ABCC8
  • Curation Notes: ClinVar Annotator: match by term: Inborn genetic diseases
  • Original References(s): PMID:10204114 PMID:10447255 PMID:10487673 PMID:10923633 PMID:11272143 PMID:11999683 PMID:12941782 PMID:14692646 PMID:14715863 PMID:15111507 PMID:15356046 PMID:15562009 PMID:15579781 PMID:15580558 PMID:15718250 PMID:15807877 PMID:15842514 PMID:16186397 PMID:16357843 PMID:16429405 PMID:16613899 PMID:16860127 PMID:16885549 PMID:17378627 PMID:18025408 PMID:18339976 PMID:18414213 PMID:18493152 PMID:18599530 PMID:18662362 PMID:18758683 PMID:18767144 PMID:18981553 PMID:19475716 PMID:20672374 PMID:20685672 PMID:20943779 PMID:21544516 PMID:21716120 PMID:21851374 PMID:21989597 PMID:22704848 PMID:22902787 PMID:23275527 PMID:23345197 PMID:24401662 PMID:24411943 PMID:24768178 PMID:24959012 PMID:25008049 PMID:25306193 PMID:25741868 PMID:25765446 PMID:25931474 PMID:25955821 PMID:25972930 PMID:26221353 PMID:26268944 PMID:26448950 PMID:26467025 PMID:27175728 PMID:27538677 PMID:27754802 PMID:27908292 PMID:27913849 PMID:28442472 PMID:28492532 PMID:31291970 PMID:31604004 PMID:32027066 PMID:32792356 PMID:32928245 PMID:33046911 PMID:33300273 PMID:33410562 PMID:34304300 PMID:34309670 PMID:34927408 PMID:35402560 PMID:36407475 PMID:7716548 PMID:8923011 PMID:9075812 PMID:9618169 PMID:9648840


  • Go Back to source page   Continue to Ontology report