Редактирование: ARPC1A

Actin-related protein 2/3 complex subunit 1A (SOP2-like protein) [SOP2L]

==Publications==

{{medline-entry
|title=Eight common genetic variants associated with serum DHEAS levels suggest a key role in ageing mechanisms.
|pubmed-url=https://pubmed.ncbi.nlm.nih.gov/21533175
|abstract=Dehydroepiandrosterone sulphate (DHEAS) is the most abundant circulating steroid secreted by adrenal glands--yet its function is unknown. Its serum concentration declines significantly with increasing age, which has led to speculation that a relative DHEAS deficiency may contribute to the development of common age-related diseases or diminished longevity. We conducted a meta-analysis of genome-wide association data with 14,846 individuals and identified eight independent common SNPs associated with serum DHEAS concentrations. Genes at or near the identified loci include [[ZKSCAN5]] (rs11761528; p = 3.15 × 10(-36)), [[SULT2A1]] (rs2637125; p =  2.61 × 10(-19)), [[ARPC1A]] (rs740160; p =  1.56 × 10(-16)), [[TRIM4]] (rs17277546; p =  4.50 × 10(-11)), [[BMF]] (rs7181230; p = 5.44 × 10(-11)), [[HHEX]] (rs2497306; p =  4.64 × 10(-9)), [[BCL2L11]] (rs6738028; p = 1.72 × 10(-8)), and [[CYP2C9]] (rs2185570; p = 2.29 × 10(-8)). These genes are associated with type 2 diabetes, lymphoma, actin filament assembly, drug and xenobiotic metabolism, and zinc finger proteins. Several SNPs were associated with changes in gene expression levels, and the related genes are connected to biological pathways linking DHEAS with ageing. This study provides much needed insight into the function of DHEAS.
|mesh-terms=* Actin-Related Protein 2-3 Complex
* Adaptor Proteins, Signal Transducing
* Adult
* Aged
* Aging
* Apoptosis Regulatory Proteins
* Aryl Hydrocarbon Hydroxylases
* Bcl-2-Like Protein 11
* Cytochrome P-450 CYP2C9
* DNA-Binding Proteins
* Dehydroepiandrosterone Sulfate
* European Continental Ancestry Group
* Female
* Gene Expression
* Genome-Wide Association Study
* Homeodomain Proteins
* Humans
* Kruppel-Like Transcription Factors
* Linkage Disequilibrium
* Liver
* Male
* Membrane Proteins
* Middle Aged
* Polymorphism, Single Nucleotide
* Proto-Oncogene Proteins
* Sulfotransferases
* Transcription Factors
* Young Adult

|full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3077384
}}