Slc30a8 rs13266634
WebJan 1, 2024 · SLC30A8 encrypts the zinc carrier protein component-8, which contains eight exons and 369 amino acids, and is considered to be the β-cell zinc homeostasis regulator. The rs13266634 polymorphism is a non-synonymous SNP that causes an amino acid transition from arginine (R/C) to tryptophan (W/T) at position 325. WebAdvertisers Access Statistics Resources. Dr Mohan Z Mani "Thank you very much for having published my article in record time.I would like to compliment you and your entire staff for your promptness, courtesy, and willingness to be customer friendly, which is quite unusual.I was given your reference by a colleague in pathology,and was able to directly phone your …
Slc30a8 rs13266634
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WebZestimate® Home Value: $728,600. 23430 8th St, Santa Clarita, CA is a single family home that contains 1,387 sq ft and was built in 1961. It contains 3 bedrooms and 2 bathrooms. … WebSlc30A8 is a zinc efflux transporter involved in the accumulation of zinc in intracellular vesicles and is expressed at a high level in the pancreas, particularly in islets of …
WebClinical characteristics were obtained for all subjects, and genotype analysis was performed by PCR-RFLP analysis. Results: Allele and genotyping frequencies, odds ratios, and 95% … WebApr 12, 2014 · rs13266634 is one of the most consistently replicated diabetes risk variants (odds ratio of 1.14 for the R allele) ( 6 ). This SNP encodes a C→T base substitution in the …
WebOct 1, 2008 · Similarly, we found no association between the SLC30A8 rs13266634 variant and type 2 diabetes, while an association with combined IFG/type 2 diabetes reached borderline significance. Interestingly, the risk allele that increased diabetes risk in Europeans was also associated with a lower BMI in this population. WebSLC30A8, CDKAL1, TCF7L2, KCNQ1 and IGF2BP2 are Associated with Type 2 Diabetes Mellitus in Iranian Patients Javascript is currently disabled in your browser. Several …
WebJun 1, 2007 · Sladek et al. (2007) identified an association between a nonsynonymous variant in SLC30A8 (arg325trp; R325W; rs13266634) and susceptibility to type 2 diabetes (T2D; 125853). The risk allele was the major C allele, which corresponds to R325.
WebSLC30A8, CDKAL1, TCF7L2, KCNQ1 and IGF2BP2 are Associated with Type 2 Diabetes Mellitus in Iranian Patients Javascript is currently disabled in your browser. Several features of this site will not function whilst javascript is disabled. news osnabrücker landWebMeta-analysis of association between SLC30A8 rs13266634 and T2DM in Chinese population [C]. Huang Qin, Dong Minghua, Li Shumei, BMEI 2012;International Conference on Biomedical Engineering and Informatics . 2012. 机译：中国人群SLC30A8基因rs13266634与T2DM相关性的Meta分析 ... newsothersmiss.comWebDec 13, 2013 · The SLC30A8 rs13266634 polymorphism is among the most confirmed genetic markers of T2D in Europeans and East Asians . The SLC30A8 gene encodes a … middle earth travelWebAug 31, 2010 · SLC30A8 encodes ion channel zinc transporter protein member 8 (ZnT-8), which is thought to be the β-cell zinc concentration regulator. ZnT-8 is a critical molecule during the insulin maturation and release process that carries zinc from the cytoplasm into insulin secretory vesicles [ 11 ]. middle-earthtm shadow of war reviewWebJul 14, 2024 · SLC30A8 rs13266634 has been reported to be associated with high zinc levels in human islets (Wong et al. 2024). To our knowledge, there is currently no report on the relationship between seminal plasma zinc concentration and zinc transporter SNP. The genetic background associated with zinc concentration is not fully understood. news osterodemiddle earth ultimate collector\u0027s editionWebSep 25, 2024 · Introduction:Published data regarding the association between solute carrier family 30, member 8 (SLC30A8) rs13266634 polymorphism and type 2 diabetes mellitus … new sotem