Symbol
| DDAH2
| contributors: mct - updated : 07-10-2015
|
HGNC name
| dimethylarginine dimethylaminohydrolase 2
|
HGNC id
| 2716
|
Other morbid association(s)
|
Type | Gene Modification | Chromosome rearrangement | Protein expression | Protein Function
|
---|
constitutional
|  
|  
| --low
|  
|
by hypermethylation in DDAH2 promoter is positively correlated to the dysfunction of endothelial progenitor cells (EPCs) in coronary artery disease patients | |
Susceptibility
|
to risk of developing myocardial infarction (MI) to chronic kidney disease |
Variant & Polymorphism
SNP
| rs805304 C allele was associated with decreased risk of MI and decreased risk of obesity |
|
rs9267551 functional variant of the DDAH2 gene is associated with chronic kidney disease with carriers of the C allele having a lower risk of renal dysfunction independently from several confounders |
|
|
Candidate gene
Marker
Therapy target
| | | |