UMOD, uromodulin, 7369

N. diseases: 164; N. variants: 35
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121917769
rs121917769
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C4511620
Disease:
Autosomal dominant tubulointerstitial kidney disease
0.010 GeneticVariation BEFREE ADTKD-<i>UMOD</i>, which is associated with retention of mutant uromodulin in the endoplasmic reticulum (ER) of renal thick ascending limb cells, is characterized by hyperuricemia, interstitial fibrosis, inflammation and renal failure, and we used targeted homologous recombination to generate a knock-in mouse model with an ADTKD-causing missense cysteine to arginine uromodulin mutation (C125R). 28325753 2017
dbSNP: rs188709583
rs188709583
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C4511620
Disease:
Autosomal dominant tubulointerstitial kidney disease
0.010 GeneticVariation BEFREE A novel heterozygous mutation (c.1648G > A,p.V550I) in exon 8 of UMOD gene was found in in a Chinese child case with ADTKD-UMOD, which extends our understanding of UMOD gene mutation spectrum and phenotype of ADTKD-UMOD in children. 31068150 2019
dbSNP: rs768597701
rs768597701
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C4511620
Disease:
Autosomal dominant tubulointerstitial kidney disease
0.010 GeneticVariation BEFREE Identification of a novel UMOD mutation (c.163G>A) in a Brazilian family with autosomal dominant tubulointerstitial kidney disease. 29513881 2018
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C2316810
Disease:
Chronic kidney disease stage 5
0.020 GeneticVariation BEFREE We tested a large cohort of Caucasian patients for association of rs12917707 with IgA nephropathy showing a benign, stable course and with IgA nephropathy that progressed toward end stage renal failure. 25163389 2014
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C2316810
Disease:
Chronic kidney disease stage 5
0.020 GeneticVariation BEFREE The rs12917707 minor allele showed association with lower risk of ESRD (OR 0.89 [0.76-1.03], p = 0.04) consistent in effect size and direction with the previous report (Böger et al, PLoS Genet 2011). 22947327 2012
dbSNP: rs13333226
rs13333226
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C2316810
Disease:
Chronic kidney disease stage 5
0.010 GeneticVariation BEFREE A common variation rs13333226 in the promoter region of UMOD gene was independently associated with ESRD in Han Chinese. 27938332 2016
dbSNP: rs183962941
rs183962941
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C2316810
Disease:
Chronic kidney disease stage 5
0.010 GeneticVariation BEFREE One SNP (rs183962941), located in a non-coding region of UMOD, was nominally associated with ESRD (p = 0.008). 28609449 2017
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C1561643
Disease:
Chronic Kidney Diseases
T 0.730 GeneticVariation GWASDB New loci associated with kidney function and chronic kidney disease. 20383146 2010
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.730 GeneticVariation BEFREE The rs12917707 was not associated with CKD. 28954491 2017
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.730 GeneticVariation BEFREE In recent genetic association studies, common variants including rs12917707 in the UMOD locus have shown strong evidence of association with eGFR, prevalent and incident chronic kidney disease and uromodulin urinary concentration in general population cohorts. 22947327 2012
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.730 GeneticVariation GWASDB Genome-wide association and functional follow-up reveals new loci for kidney function. 22479191 2012
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.730 GeneticVariation BEFREE The genetic rs12917707-G>T variant in uromodulin (UMOD) has been associated with renal function, chronic kidney disease and hypertension with the minor T-allele showing a protective effect. 28418009 2018
dbSNP: rs12922822
rs12922822
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.700 GeneticVariation GWASDB Genetic association for renal traits among participants of African ancestry reveals new loci for renal function. 21931561 2011
dbSNP: rs4293393
rs4293393
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C1561643
Disease:
Chronic Kidney Diseases
0.010 GeneticVariation BEFREE We observed an association between CKD and a variant with 80% population frequency, rs4293393-T, positioned next to the UMOD gene (GeneID: 7369) on chromosome 16p12 (OR = 1.25, P = 4.1x10(-10)). 20686651 2010
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
T 0.700 GeneticVariation GWASCAT New loci associated with kidney function and chronic kidney disease. 20383146 2010
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016
dbSNP: rs13329952
rs13329952
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016
dbSNP: rs188709583
rs188709583
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
0.700 GeneticVariation GWASCAT Identification of CDC42BPG as a novel susceptibility locus for hyperuricemia in a Japanese population. 29124443 2018
dbSNP: rs13333226
rs13333226
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0011847
Disease:
Diabetes
0.710 GeneticVariation GWASCAT A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. 29703844 2018
dbSNP: rs13333226
rs13333226
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0011847
Disease:
Diabetes
0.710 GeneticVariation BEFREE The G allele of rs13333226 was associated with a decreased risk of nephropathy [odds ratio (OR) 0.80, 95% confidence interval (CI) 0.69-0.91, P = 0.001] after correction for confounding factors like age, sex, body mass index (BMI), blood pressure, kidney function, smoking and duration of diabetes. 21738052 2011
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0011847
Disease:
Diabetes
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016
dbSNP: rs12922822
rs12922822
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0011847
Disease:
Diabetes
T 0.700 GeneticVariation GWASCAT Mapping eGFR loci to the renal transcriptome and phenome in the VA Million Veteran Program. 31451708 2019
dbSNP: rs13333226
rs13333226
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0011849
Disease:
Diabetes Mellitus
0.710 GeneticVariation BEFREE The G allele of rs13333226 was associated with a decreased risk of nephropathy [odds ratio (OR) 0.80, 95% confidence interval (CI) 0.69-0.91, P = 0.001] after correction for confounding factors like age, sex, body mass index (BMI), blood pressure, kidney function, smoking and duration of diabetes. 21738052 2011
dbSNP: rs13333226
rs13333226
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0011849
Disease:
Diabetes Mellitus
0.710 GeneticVariation GWASCAT A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes. 29703844 2018
dbSNP: rs12917707
rs12917707
Entrez Id: 7369
Gene Symbol: UMOD
UMOD
CUI: C0011849
Disease:
Diabetes Mellitus
T 0.700 GeneticVariation GWASCAT Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function. 26831199 2016