IRX1, iroquois homeobox 1, 79192

N. diseases: 28; N. variants: 2
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.100 GeneticVariation phenotype GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
CUI: C0017654
Disease: Glomerular Filtration Rate
Glomerular Filtration Rate
0.100 GeneticVariation phenotype GWASCAT Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis. 31015462 2019
CUI: C0205682
Disease: Waist-Hip Ratio
Waist-Hip Ratio
0.100 GeneticVariation phenotype GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.080 GeneticVariation group BEFREE In a recent study, we identified five tumor suppressive genes (IRX1, EBF3, SLC5A8, SEPT9, and FUSSEL18) as frequently methylated in HNSCC biopsies using a global methylation analysis via restriction landmark genomic scanning. 20029986 2010
CUI: C0730294
Disease: North Carolina macular dystrophy
North Carolina macular dystrophy
0.020 GeneticVariation disease BEFREE Duplication events downstream of IRX1 cause North Carolina macular dystrophy at the MCDR3 locus. 28790370 2017
CUI: C0010068
Disease: Coronary heart disease
Coronary heart disease
0.010 GeneticVariation disease BEFREE In addition, the results suggest that genetic variants of the IRX1 gene may contribute to the pathogenesis of CHD. 28358424 2017
CUI: C0024115
Disease: Lung diseases
Lung diseases
0.300 Biomarker group CTD_human Expression of Iroquois genes is up-regulated during early lung development in the nitrofen-induced pulmonary hypoplasia. 21238641 2011
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.080 Biomarker group BEFREE Homeobox gene IRX1 is a tumor suppressor gene in gastric carcinoma. 20440264 2010
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.080 Biomarker group BEFREE IRX1 is a newly identified tumor suppressor gene and hypermethylation involves the decreased expression in gastric cancer. 22934698 2013
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.080 Biomarker group BEFREE Here, we use homozygous knockout mutants of zebrafish to demonstrate that the IRX1 gene is a true tumor suppressor gene and mechanism of the tumor suppression is mediated by repressing cell cycle progression. 31450023 2019
CUI: C0027651
Disease: Neoplasms
Neoplasms
0.080 Biomarker group BEFREE In serum from osteosarcoma patients, the presence of IRX1 hypomethylation in circulating tumor DNA reduced lung metastasis-free survival. 25822025 2015
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.050 Biomarker disease BEFREE IRX1, SOX1 and MSX1 with risk associated SNP loci may serve as candidate biomarkers for diagnosis and prognosis of GC. 25982683 2015
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.050 Biomarker disease BEFREE Here, we identified protein arginine methyltransferase 5 (PRMT5) as a major upstream regulator of IRX1 for determining GC progression. 29802960 2018
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.050 Biomarker disease BEFREE IRX1 influences peritoneal spreading and metastasis via inhibiting BDKRB2-dependent neovascularization on gastric cancer. 21602894 2011
CUI: C0699791
Disease: Stomach Carcinoma
Stomach Carcinoma
0.050 Biomarker disease BEFREE Homeobox gene IRX1 is a tumor suppressor gene in gastric carcinoma. 20440264 2010
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.040 Biomarker disease BEFREE Here, we identified protein arginine methyltransferase 5 (PRMT5) as a major upstream regulator of IRX1 for determining GC progression. 29802960 2018
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.040 Biomarker disease BEFREE IRX1 influences peritoneal spreading and metastasis via inhibiting BDKRB2-dependent neovascularization on gastric cancer. 21602894 2011
CUI: C0024623
Disease: Malignant neoplasm of stomach
Malignant neoplasm of stomach
0.040 Biomarker disease BEFREE IRX1, SOX1 and MSX1 with risk associated SNP loci may serve as candidate biomarkers for diagnosis and prognosis of GC. 25982683 2015
CUI: C0027627
Disease: Neoplasm Metastasis
Neoplasm Metastasis
0.030 Biomarker phenotype BEFREE Together, these results identify IRX1 as a prometastatic gene, implicate IRX1 hypomethylation as a potential molecular marker for lung metastasis, and suggest that epigenetic reversion of IRX1 activation may be beneficial for controlling osteosarcoma metastasis. 25822025 2015
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.020 Biomarker disease BEFREE Hypermethylation of EBF3 and IRX1 genes in synovial fibroblasts of patients with rheumatoid arthritis. 23456299 2013
CUI: C0003873
Disease: Rheumatoid Arthritis
Rheumatoid Arthritis
0.020 Biomarker disease BEFREE Our findings indicate that IRX1 and HLA-DRB1 are the strongest genetic factors for RF production in RA. 26815016 2016
Secondary malignant neoplasm of lung
0.020 Biomarker disease BEFREE As results, the remarkable suppression on peritoneal spreading and pulmonary metastasis of SGC-7901 cells by IRX1 transfectant correlates to reduced angiogenesis as well as VM formation. 21602894 2011
Secondary malignant neoplasm of lung
0.020 Biomarker disease BEFREE Together, these results identify IRX1 as a prometastatic gene, implicate IRX1 hypomethylation as a potential molecular marker for lung metastasis, and suggest that epigenetic reversion of IRX1 activation may be beneficial for controlling osteosarcoma metastasis. 25822025 2015
CUI: C0596263
Disease: Carcinogenesis
Carcinogenesis
0.020 Biomarker phenotype BEFREE In this study, we found that knockout of zebrafish Irx1 gene induced hyperplasia and tumorigenesis in the multiple organs where the gene was expressed. 31450023 2019
CUI: C0730294
Disease: North Carolina macular dystrophy
North Carolina macular dystrophy
0.020 Biomarker disease BEFREE The 5 mutations V1 to V5 segregated perfectly in the 102 affected and 39 unaffected members of the 12 NCMD families. 26507665 2016