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GENE - TERM ANNOTATION REPORT

RGD ID: 18929904
Species: Heterocephalus glaber
RGD Object: Gene
Symbol: Slc11a1
Name: solute carrier family 11 member 1
Acc ID: DOID:8778
Term: Crohn's disease
Definition: An intestinal disease that involves inflammation located_in intestine. (DO)
Definition Source(s): http://en.wikipedia.org/wiki/Chron%27s_disease "DO" "DO", https://www.genome.gov/Genetic-Disorders/Crohns-Disease "DO" "DO"
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 SymbolQualifierEvidenceWithReferenceSourceNotesOriginal Reference(s)
Slc11a1 ISOSLC11A1 (Homo sapiens)9068941RGDDNA:insertion/deletion:3' utr (human)PMID:18340647 REF_RGD_ID:5684939
Slc11a1 ISOSLC11A1 (Homo sapiens)9068941RGDDNA:point mutation:promoter:-237C>T (human)PMID:16059695 REF_RGD_ID:5684952
Slc11a1 ISOSLC11A1 (Homo sapiens)9068941RGDDNA:polymorphism: :823C>T (human)PMID:17131479 REF_RGD_ID:5684942
Slc11a1 ISOSLC11A1 (Homo sapiens)9068941RGDDNA:polymorphism:promoter (human)PMID:11929588 REF_RGD_ID:5684968
Slc11a1 ISOSLC11A1 (Homo sapiens)9068941RGDDNA:repeat, polymorphisms:promoter, intron:p.D543N (human)PMID:18454481 REF_RGD_ID:5684938
Slc11a1no_associationISOSLC11A1 (Homo sapiens)9068941RGDDNA:polymorphism:promoter (human)PMID:15757519 REF_RGD_ID:5684956
Slc11a1no_associationISOSLC11A1 (Homo sapiens)9068941RGDDNA:polymorphisms:promoter (human)PMID:17385031 REF_RGD_ID:5684941
Slc11a1 ISOSLC11A1 (Homo sapiens)9068941CTDCTD Direct Evidence: marker/mechanismPMID:16059695
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