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GENE - TERM ANNOTATION REPORT

3 Annotations Found.

An association has been curated linking XRCC1 and Esophageal carcinoma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Huang X, etal., Oncol Lett. 2017 Feb;13(2):704-714. doi: 10.3892/ol.2016.5496. Epub 2016 Dec 14.
  • 3 additional annotations were made from Huang X, etal., Oncol Lett. 2017 Feb;13(2):704-714. doi: 10.3892/ol.2016.5496. Epub 2016 Dec 14.
  • 39 RGD objects have been annotated to Esophageal carcinoma  (HP:0011459)
  • 124 papers in RGD have been used to annotate XRCC1
  • Qualifier: treatment


    • An association has been curated linking XRCC1 and Esophageal carcinoma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Zhang Y, etal., Oncol Lett. 2016 May;11(5):3508-3514. doi: 10.3892/ol.2016.4384. Epub 2016 Mar 29.
  • 3 additional annotations were made from Zhang Y, etal., Oncol Lett. 2016 May;11(5):3508-3514. doi: 10.3892/ol.2016.4384. Epub 2016 Mar 29.
  • 39 RGD objects have been annotated to Esophageal carcinoma  (HP:0011459)
  • 124 papers in RGD have been used to annotate XRCC1
  • Qualifier: treatment
  • Curation Notes: DNA:SNPs:exon 6, exon 9, exon 10:multiple (human)


    • An association has been curated linking XRCC1 and Esophageal carcinoma in Homo sapiens.        

  • The association was inferred by association of genotype and phenotype (IAGP)
    		•  
  • The annotation was made from Chen XQ, etal., Braz J Med Biol Res. 2013 Dec;46(12):1028-1032. doi: 10.1590/1414-431X20133396. Epub 2013 Dec 2.
  • 3 additional annotations were made from Chen XQ, etal., Braz J Med Biol Res. 2013 Dec;46(12):1028-1032. doi: 10.1590/1414-431X20133396. Epub 2013 Dec 2.
  • 39 RGD objects have been annotated to Esophageal carcinoma  (HP:0011459)
  • 124 papers in RGD have been used to annotate XRCC1
  • Qualifier: susceptibility
  • Curation Notes: DNA:missense mutation:exon 9: p.T304A, c.910A>G (human)


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