NMU, neuromedin U, 10874

N. diseases: 68; N. variants: 5
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3805382
rs3805382
Entrez Id: 10874
Gene Symbol: NMU
NMU
CUI: C0001925
Disease:
Albuminuria
A 0.700 GeneticVariation GWASCAT Genetic Association of Albuminuria with Cardiometabolic Disease and Blood Pressure. 30220432 2018
dbSNP: rs149106723
rs149106723
Entrez Id: 10874
Gene Symbol: NMU
NMU
CUI: C2362324
Disease:
Pediatric Obesity
0.020 GeneticVariation BEFREE Compared with NMU-25, NMS had a significantly reduced maximum response in saphenous vein, and the Arg165Trp variant of NMU-25, associated with childhood-onset obesity, was without effect. 18987052 2009
dbSNP: rs149106723
rs149106723
Entrez Id: 10874
Gene Symbol: NMU
NMU
CUI: C2362324
Disease:
Pediatric Obesity
0.020 GeneticVariation BEFREE The rare NMU Arg165Trp variant cosegregated with childhood obesity in a Czech family. 16984985 2006
dbSNP: rs12500837
rs12500837
Entrez Id: 10874
Gene Symbol: NMU
NMU
CUI: C2362324
Disease:
Pediatric Obesity
0.010 GeneticVariation BEFREE From a large European multi-center study on childhood obesity, 4,528 children (2.0-9.9 years, mean age 6.0±1.8 SD; boys 52.2%) were randomly selected, stratifying by age, sex and country, and genotyped for tag single nucleotide polymorphisms (SNPs; rs6827359, T:C; rs12500837, T:C; rs9999653,C:T) of NMU gene, then haplotypes were inferred. 28235053 2017
dbSNP: rs6827359
rs6827359
Entrez Id: 10874
Gene Symbol: NMU
NMU
CUI: C2362324
Disease:
Pediatric Obesity
0.010 GeneticVariation BEFREE From a large European multi-center study on childhood obesity, 4,528 children (2.0-9.9 years, mean age 6.0±1.8 SD; boys 52.2%) were randomly selected, stratifying by age, sex and country, and genotyped for tag single nucleotide polymorphisms (SNPs; rs6827359, T:C; rs12500837, T:C; rs9999653,C:T) of NMU gene, then haplotypes were inferred. 28235053 2017
dbSNP: rs9999653
rs9999653
Entrez Id: 10874
Gene Symbol: NMU
NMU
CUI: C2362324
Disease:
Pediatric Obesity
0.010 GeneticVariation BEFREE From a large European multi-center study on childhood obesity, 4,528 children (2.0-9.9 years, mean age 6.0±1.8 SD; boys 52.2%) were randomly selected, stratifying by age, sex and country, and genotyped for tag single nucleotide polymorphisms (SNPs; rs6827359, T:C; rs12500837, T:C; rs9999653,C:T) of NMU gene, then haplotypes were inferred. 28235053 2017