Gene Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 GeneticVariation disease BEFREE Polymorphisms in the human Slc11a1/Nramp1 gene have been associated with host susceptibility to leprosy. 26814595 2016
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 GeneticVariation disease BEFREE Genetic factors, such as the vitamin D receptor, the major histocompatibility complex region, chromosome 20, human toll-like receptors, the natural resistance-associated macrophage protein 1, the nucleotide-binding oligomerization domain containing 2, phosphate-regulating gene with homologies to endopeptidase on the X chromosome and the tyrosine kinase growth factor receptor-ErbB-2, contribute to both vitamin D status and leprosy. 22170299 2012
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 Biomarker disease CTD_human Iron and infection: effects of host iron status and the iron-regulatory genes haptoglobin and NRAMP1 (SLC11A1) on host-pathogen interactions in tuberculosis and HIV. 16597321 2006
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 GeneticVariation disease BEFREE Thus, variation in or near the NRAMP1 gene may exert an influence on the clinical presentation of leprosy, possibly by influencing cellular immune response type. 11791966 2001
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 GeneticVariation disease BEFREE In the homologous human NRAMP1 gene, a total of 11 polymorphisms have been identified, which are being used to test for the linkage of NRAMP1 alleles with human responses to mycobacteria, including susceptibility to tuberculosis and leprosy, as well as BCG immunotherapy in bladder cancer. 11010829 2000
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 GeneticVariation disease BEFREE A sib-pair linkage analysis between the Mitsuda response and the NRAMP1 gene was done among 20 nuclear families with leprosy (totaling 118 sibs) from Ho Chi Minh City, Vietnam. 10608779 2000
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 Biomarker disease BEFREE Several studies now provide evidence for a role for NRAMP1 in determining human susceptibility to autoimmune (rheumatoid arthritis. juvenile rheumatoid arthritis, diabetes, Crohn's disease) and infectious (tuberculosis, leprosy) diseases.Amongst these. data are accumulating to support the hypothesis that a functional Z-DNA forming repeat polymorphism in the promoter region of human NRAMP1 contributes directly to disease susceptibility. 10065630 1999
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 GeneticVariation disease BEFREE This finding is consistent with the hypothesis that NRAMP1 itself is a leprosy susceptibility locus. 9419180 1998
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 GeneticVariation disease BEFREE Through comparative genomics, we have identified the homologous human NRAMP1 gene, alleles of which are now being used for tests of linkage with TB and leprosy. 9509263 1998
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
0.390 GeneticVariation disease BEFREE Recent genetic studies have found that allelic variants at the human NRAMP1 locus are associated with susceptibility to leprosy (Mycobacterium leprae) and tuberculosis (Mycobacterium tuberculosis) and possibly with the onset of rheumatoid arthritis. 9719491 1998