JP2010088342A5 - - Google Patents

Download PDF

Info

Publication number
JP2010088342A5
JP2010088342A5 JP2008261318A JP2008261318A JP2010088342A5 JP 2010088342 A5 JP2010088342 A5 JP 2010088342A5 JP 2008261318 A JP2008261318 A JP 2008261318A JP 2008261318 A JP2008261318 A JP 2008261318A JP 2010088342 A5 JP2010088342 A5 JP 2010088342A5
Authority
JP
Japan
Prior art keywords
snp
gene
polymorphism
risk
type
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
JP2008261318A
Other languages
Japanese (ja)
Other versions
JP2010088342A (en
Filing date
Publication date
Application filed filed Critical
Priority to JP2008261318A priority Critical patent/JP2010088342A/en
Priority claimed from JP2008261318A external-priority patent/JP2010088342A/en
Publication of JP2010088342A publication Critical patent/JP2010088342A/en
Publication of JP2010088342A5 publication Critical patent/JP2010088342A5/ja
Pending legal-status Critical Current

Links

Claims (5)

高血圧発症に関する一塩基多型(SNP)マーカーの使用方法であって、
前記高血圧発症に関するSNPマーカーは、RGS2遺伝子におけるA/G多型SNP(rs番号:rs3767489)、ADD1遺伝子におけるC/A多型SNP(rs番号:rs4961)、CACNA2D2遺伝子におけるA/G多型SNP(rs番号:rs2236957)、及び、CAT遺伝子におけるC/T多型SNP(rs番号:rs769214)からなる群から選択される少なくとも2つのSNPsからなり、
被検試料を準備する準備工程と、前記被検試料について前記少なくとも2つのSNPsをタイピングするタイピング工程と、前記タイピング工程の結果に基づき高血圧発症のリスクを判定する判定工程とを含み、
前記判定工程における判定が、前記RGS2遺伝子のSNPのリスク多型をAA型、前記ADD1遺伝子のSNPのリスク多型をAA型、前記CACNA2D2遺伝子のSNPのリスク多型をAA型、及び、前記CAT遺伝子のSNPのリスク多型をTT型及びTC型とし、前記リスク多型の数が増加するほど高血圧発症のリスクが増加すると判定することを含む、高血圧発症に関するSNPマーカーの使用方法。
A method of using a single nucleotide polymorphism (SNP) marker for the development of hypertension comprising:
The SNP markers related to the onset of hypertension are the A / G polymorphism SNP (rs number: rs3767489) in the RGS2 gene, the C / A polymorphism SNP (rs number: rs4961) in the ADD1 gene, and the A / G polymorphism SNP in the CACNA2D2 gene ( rs number: rs2236957) and at least two SNPs selected from the group consisting of C / T polymorphic SNPs in the CAT gene (rs number: rs769214),
A preparation step of preparing a test sample, seen containing a typing step of typing said at least two SNPs for the test sample, and a determination step of determining the risk of developing hypertension based on the result of the typing process,
In the determination step, the SNP risk polymorphism of the RGS2 gene is AA type, the SNP risk polymorphism of the ADD1 gene is AA type, the SNP risk polymorphism of the CACNA2D2 gene is AA type, and the CAT A method of using an SNP marker for the development of hypertension , comprising determining that the risk polymorphism of a gene SNP is a TT type and a TC type, and that the risk of developing hypertension increases as the number of the risk polymorphism increases .
請求項1記載の高血圧発症に関するSNPマーカーの使用方法に使用するSNPマーカーであって、RGS2遺伝子におけるA/G多型SNP(rs番号:rs3767489)、ADD1遺伝子におけるC/A多型SNP(rs番号:rs4961)、CACNA2D2遺伝子におけるA/G多型SNP(rs番号:rs2236957)、及び、CAT遺伝子におけるC/T多型SNP(rs番号:rs769214)からなる群から選択される少なくとも2つからなるSNPマーカー。 It is a SNP marker used for the usage method of the SNP marker regarding the onset of hypertension of Claim 1, Comprising: A / G polymorphism SNP (rs number: rs3766789) in RGS2 gene, C / A polymorphism SNP (rs number) in ADD1 gene : Rs4961), A / G polymorphic SNP in the CACNA2D2 gene (rs number: rs2236957), and C / T polymorphic SNP in the CAT gene (rs number: rs769214). marker. 高血圧の発症リスクを検査するキットであって、RGS2遺伝子におけるA/G多型SNP(rs番号:rs3767489)、ADD1遺伝子におけるC/A多型SNP(rs番号:rs4961)、CACNA2D2遺伝子におけるA/G多型SNP(rs番号:rs2236957)、及び、CAT遺伝子におけるC/T多型SNP(rs番号:rs769214)からなる群から選択される少なくとも2つからなる高血圧発症に関するSNPマーカーのSNPsをタイピングするためのポリヌクレオチド、プライマー、プローブ、及びDNAマイクロアレイの少なくとも1つを含む、高血圧発症リスク検査キット。   A kit for examining the risk of developing hypertension, comprising an A / G polymorphism SNP in RGS2 gene (rs number: rs3767489), a C / A polymorphism SNP in ADD1 gene (rs number: rs4961), and an A / G in CACNA2D2 gene To type SNPs of SNP markers related to hypertension comprising at least two selected from the group consisting of a polymorphic SNP (rs number: rs2236957) and a C / T polymorphic SNP (rs number: rs769214) in the CAT gene A hypertension risk test kit comprising at least one of a polynucleotide, a primer, a probe, and a DNA microarray. さらに、説明書を含み、前記説明書には、前記RGS2遺伝子のSNP(rs番号:rs3767489)のリスク多型をAA型、前記ADD1遺伝子のSNP(rs番号:rs4961)のリスク多型をAA型、前記CACNA2D2遺伝子のSNP(rs番号:rs2236957)のリスク多型をAA型、及び、前記CAT遺伝子のSNP(rs番号:rs769214)のリスク多型をTT型及びTC型とし、リスク多型の保有数の増加にともない高血圧発症のリスクが高まることが記載される、請求項3記載の高血圧発症リスク検査キット。 In addition, the instructions include a risk polymorphism of the RGS2 gene SNP (rs number: rs3767489) type AA, and a risk polymorphism of the ADD1 gene SNP (rs number: rs4961) type AA. The risk polymorphism of the SAC (rs number: rs2236957) of the CACNA2D2 gene is AA type, and the risk polymorphism of the SNP (rs number: rs769214) of the CAT gene is TT type and TC type. The hypertension risk test kit according to claim 3 , wherein the risk of developing hypertension increases as the number increases. 高血圧発症に関する一塩基多型(SNP)マーカーの使用方法であって、
前記高血圧発症に関するSNPマーカーは、RGS2遺伝子におけるA/G多型SNP(rs番号:rs3767489)と連鎖不均衡を示すSNP、ADD1遺伝子におけるC/A多型SNP(rs番号:rs4961)と連鎖不均衡を示すSNP、CACNA2D2遺伝子におけるA/G多型SNP(rs番号:rs2236957)と連鎖不均衡を示すSNP、及び、CAT遺伝子におけるC/T多型SNP(rs番号:rs769214)と連鎖不均衡を示すSNPからなる群から選択される少なくとも2つのSNPsからなり、
被検試料を準備する準備工程と、前記被検試料について前記少なくとも2つのSNPsをタイピングするタイピング工程と、前記タイピング工程の結果に基づき高血圧発症のリスクを判定する判定工程とを含み、
前記判定工程における判定が、前記RGS2遺伝子のSNPのリスク多型をAA型、前記ADD1遺伝子のSNPのリスク多型をAA型、前記CACNA2D2遺伝子のSNPのリスク多型をAA型、及び、前記CAT遺伝子のSNPのリスク多型をTT型及びTC型とし、前記リスク多型と連鎖する多型の数が増加するほど高血圧発症のリスクが増加すると判定することを含む、高血圧発症に関するSNPマーカーの使用方法。
A method of using a single nucleotide polymorphism (SNP) marker for the development of hypertension comprising:
The SNP marker related to the development of hypertension is a SNP showing linkage disequilibrium with the A / G polymorphism SNP (rs number: rs3767489) in the RGS2 gene, and a linkage disequilibrium with C / A polymorphism SNP (rs number: rs4961) in the ADD1 gene. SNP showing A, G polymorphism SNP (rs number: rs2236957) in CACNA2D2 gene and linkage disequilibrium with SNP showing C / T polymorphism SNP (rs number: rs769214) in CAT gene Consisting of at least two SNPs selected from the group consisting of SNPs;
A preparation step of preparing a test sample, seen containing a typing step of typing said at least two SNPs for the test sample, and a determination step of determining the risk of developing hypertension based on the result of the typing process,
In the determination step, the SNP risk polymorphism of the RGS2 gene is AA type, the SNP risk polymorphism of the ADD1 gene is AA type, the SNP risk polymorphism of the CACNA2D2 gene is AA type, and the CAT Use of a SNP marker for the development of hypertension , comprising determining that the risk polymorphism of a gene SNP is TT type and TC type, and that the risk of developing hypertension increases as the number of polymorphisms linked to the risk polymorphism increases Method.
JP2008261318A 2008-10-08 2008-10-08 Single nucleotide polymorphism (snp) marker associated with onset of hypertension, and use of the same Pending JP2010088342A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2008261318A JP2010088342A (en) 2008-10-08 2008-10-08 Single nucleotide polymorphism (snp) marker associated with onset of hypertension, and use of the same

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2008261318A JP2010088342A (en) 2008-10-08 2008-10-08 Single nucleotide polymorphism (snp) marker associated with onset of hypertension, and use of the same

Publications (2)

Publication Number Publication Date
JP2010088342A JP2010088342A (en) 2010-04-22
JP2010088342A5 true JP2010088342A5 (en) 2011-11-24

Family

ID=42251721

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2008261318A Pending JP2010088342A (en) 2008-10-08 2008-10-08 Single nucleotide polymorphism (snp) marker associated with onset of hypertension, and use of the same

Country Status (1)

Country Link
JP (1) JP2010088342A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR102039529B1 (en) * 2019-01-31 2019-11-01 주식회사 에스씨엘헬스케어 Single nucleotide polymorphism for predicting the risk factor of metabolic syndrome and the use thereof

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2007143504A (en) * 2005-11-29 2007-06-14 Ehime Univ Gene marker of hypertension

Similar Documents

Publication Publication Date Title
JP2010520745A5 (en)
JP2012503985A5 (en)
JP2010507388A5 (en)
JP2010527603A5 (en)
JP2010508042A5 (en)
JP2007529218A5 (en)
TWI527905B (en) Method of snp detection by using gene detection technique in bead-based microfluidics
JP2008237139A (en) Nucleic acid primer set and nucleic acid probe for detecting genotype of methylene tetrahydrofolate reductase (mthfr)
JP2010527598A5 (en)
JP2011528903A5 (en)
JP2010528590A5 (en)
JP4490988B2 (en) Nucleic acid primer set and kit for detecting genotype of serum amyloid A1 (SAA1), and detection method using the primer set
JP2009526524A5 (en)
JP2011530312A5 (en)
JP4410269B2 (en) Nucleic acid primer set, kit for detecting genotype of N-acetyltransferase 2 (NAT2), and detection method using the primer set
RU2018122965A (en) IMPROVED METHOD AND KIT FOR DETERMINING SEVERITY AND PROGRESSING PERIODONTAL DISEASE
JP2009516516A (en) Methods and probes for identifying nucleotide sequences
JP2010510804A5 (en)
JP2010035532A (en) Method for allele-specific pcr
JP2013074888A (en) METHOD FOR DETECTING MUTATION AT GENE IL28B (rs8099917) AND ITPA(rs1127354)
Vlachou et al. Development of a three-biosensor panel for the visual detection of thrombophilia-associated mutations
JP2010088342A5 (en)
KR101724130B1 (en) Biomarkers for Diagnosing Intestinal Behcet's Disease and Uses Thereof
JP2009232707A (en) Method for detecting single nucleotide polymorphism and probe-immobilized carrier
JP2007514417A5 (en)