GENE - TERM ANNOTATION REPORT
Note: Use of the qualifier "multiple interactions" designates that the annotated interaction
is comprised of a complex set of reactions and/or regulatory events, possibly involving
additional chemicals and/or gene products.
Object Symbol | Qualifier | Evidence | With | Reference | Source | Notes | Original Reference(s) | XRCC1 | ameliorates | ISO | XRCC1 (Homo sapiens) | 9068941 | RGD | DNA:missense mutation:CDS:p.R399Q (human) | PMID:23604281 REF_RGD_ID:150530625 | XRCC1 | disease_progression | ISO | XRCC1 (Homo sapiens) | 9068941 | RGD | DNA:SNP:exon 10: p.R399Q, 399G>A(human) | PMID:21378360 REF_RGD_ID:150540335 | XRCC1 | susceptibility | ISO | XRCC1 (Homo sapiens) | 9068941 | RGD | DNA:SNP:: p.R194W (human) | PMID:27706710 REF_RGD_ID:150530630 | XRCC1 | susceptibility | ISO | XRCC1 (Homo sapiens) | 9068941 | RGD | DNA:SNPs:exon 6, exon 10: C>T p.R194W, G>A p.R399Q (human) | PMID:27221877 REF_RGD_ID:150537038 | XRCC1 | susceptibility | ISO | XRCC1 (Homo sapiens) | 9068941 | RGD | DNA:SNPs:exon 9, exon 17: c.910A>G, c.1804C>A (human) | PMID:23983608 REF_RGD_ID:150530647 | XRCC1 | treatment | ISO | XRCC1 (Homo sapiens) | 9068941 | RGD | DNA:missense mutation:cds: p.R194W (human) | PMID:20331623 REF_RGD_ID:151232294 | XRCC1 | treatment | ISO | XRCC1 (Homo sapiens) | 9068941 | RGD | DNA:missense mutation:cds: p.R399Q G>A (human) | PMID:17593927 REF_RGD_ID:150573705 | XRCC1 | treatment | ISO | XRCC1 (Homo sapiens) | 9068941 | RGD | DNA:SNP: 399A>G (human) | PMID:26770441 REF_RGD_ID:150530623 | |
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