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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking SLC2A1 and childhood absence epilepsy in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
  •  
  • The annotation was made from Larsen J, etal., Epilepsia. 2015 Dec;56(12):e203-8. doi: 10.1111/epi.13222. Epub 2015 Nov 5.
  • 2 additional annotations were made from Larsen J, etal., Epilepsia. 2015 Dec;56(12):e203-8. doi: 10.1111/epi.13222. Epub 2015 Nov 5.
  • 32 CRRD objects have been annotated to childhood absence epilepsy  (DOID:1825)
  • 43 papers in CRRD have been used to annotate SLC2A1
  • Qualifier: onset
  • Curation Notes: DNA:deletion, missense mutations, SNP:multiple


  • An association has been curated linking Slc2a1 and childhood absence epilepsy in Rattus norvegicus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Larsen J, etal., Epilepsia. 2015 Dec;56(12):e203-8. doi: 10.1111/epi.13222. Epub 2015 Nov 5.
  • The annotation has been inferred from sequence orthology with SLC2A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Larsen J, etal., Epilepsia. 2015 Dec;56(12):e203-8. doi: 10.1111/epi.13222. Epub 2015 Nov 5.
  • 32 CRRD objects have been annotated to childhood absence epilepsy  (DOID:1825)
  • 73 papers in CRRD have been used to annotate Slc2a1
  • Qualifier: onset
  • Curation Notes: DNA:deletion, missense mutations, SNP:multiple


  • An association has been curated linking Slc2a1 and childhood absence epilepsy in Mus musculus.        

  • The association was inferred from sequence orthology (ISO)
  •  
  • The annotation was made from Larsen J, etal., Epilepsia. 2015 Dec;56(12):e203-8. doi: 10.1111/epi.13222. Epub 2015 Nov 5.
  • The annotation has been inferred from sequence orthology with SLC2A1 (Homo sapiens) [(IAGP) inferred by association of genotype and phenotype]
  • 2 additional annotations were made from Larsen J, etal., Epilepsia. 2015 Dec;56(12):e203-8. doi: 10.1111/epi.13222. Epub 2015 Nov 5.
  • 32 CRRD objects have been annotated to childhood absence epilepsy  (DOID:1825)
  • 46 papers in CRRD have been used to annotate Slc2a1
  • Qualifier: onset
  • Curation Notes: DNA:deletion, missense mutations, SNP:multiple


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    RGD is funded by grant HL64541 from the National Heart, Lung, and Blood Institute on behalf of the NIH.