General Information:
Id: | 2,496 |
Diseases: |
Diabetes mellitus, type II
- [OMIM]
Insulin resistance |
Homo sapiens | |
article | |
Reference: | Orho-Melander M et al.(2008) Common missense variant in the glucokinase regulatory protein gene is associated with increased plasma triglyceride and C-reactive protein but lower fasting glucose concentrations. Diabetes 57: 3112-3121 [PMID: 18678614] |
Interaction Information:
Comment | GCKR rs780094 is associated with opposite effects on fasting plasma triglyceride and glucose concentrations. In addition, we confirmed recent reports that the same SNP is associated with C-reactive protein (CRP) level. |
Formal Description Interaction-ID: 23259 |
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Comment | GCKR rs780094 is associated with opposite effects on fasting plasma triglyceride and glucose concentrations. In addition, we confirmed recent reports that the same SNP is associated with C-reactive protein (CRP) level. |
Formal Description Interaction-ID: 23263 |
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Comment | GCKR rs780094 is associated with opposite effects on fasting plasma triglyceride and glucose concentrations. In addition, we confirmed recent reports that the same SNP is associated with C-reactive protein (CRP) level. |
Formal Description Interaction-ID: 23264 |
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Comment | Both fine-mapping approaches revealed a common missense GCKR variant (rs1260326, Pro446Leu) which was strongly associated with CRP levels. |
Formal Description Interaction-ID: 23265 |
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Comment | GCKR coding SNP rs1260326 (Pro446Leu) gave the strongest signal for triglyceride concentrations in the associated interval on chromosome 2p23. |
Formal Description Interaction-ID: 23266 |
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Comment | Neither rs780094 nor rs1260326 predicted CVD. The results were similar when age, sex, LDL cholesterol, HDL cholesterol, triglycerides, BMI, sBP, dBP, smoking, family history of myocardial infarction, lipid-lowering medication, antihypertensive medication, and CRP were included as covariates. |
Formal Description Interaction-ID: 23267 |
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Comment | Neither rs780094 nor rs1260326 predicted CVD. The results were similar when age, sex, LDL cholesterol, HDL cholesterol, triglycerides, BMI, sBP, dBP, smoking, family history of myocardial infarction, lipid-lowering medication, antihypertensive medication, and CRP were included as covariates. |
Formal Description Interaction-ID: 23268 |
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Comment | In a modest number of liver samples (n = 60), neither rs780094 nor Pro446Leu genotype was associated with transcript levels of GCK or GCKR. |
Formal Description Interaction-ID: 23269 |
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Drugbank entries | Show/Hide entries for GCK |
Comment | In a modest number of liver samples (n = 60), neither rs780094 nor Pro446Leu genotype was associated with transcript levels of GCK or GCKR. |
Formal Description Interaction-ID: 23270 |
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Drugbank entries | Show/Hide entries for GCK |
Comment | In a modest number of liver samples (n = 60), neither rs780094 nor Pro446Leu genotype was associated with transcript levels of GCK or GCKR. |
Formal Description Interaction-ID: 23271 |
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Comment | In a modest number of liver samples (n = 60), neither rs780094 nor Pro446Leu genotype was associated with transcript levels of GCK or GCKR. |
Formal Description Interaction-ID: 23272 |
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Comment | At GCKR Pro446Leu, the variant allele is associated with higher triglycerides and higher CRP levels but also with a favorable metabolic marker, namely decreased glucose. |
Formal Description Interaction-ID: 23273 |
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