General Information:
Id: | 10,888 |
Diseases: |
Cardiovascular disease
Inflammation |
Homo sapiens | |
Han Chinese population in Taiwan | |
article | |
Reference: | Lin YJ et al.(2015) Genetic variants in PLCB4/PLCB1 as susceptibility loci for coronary artery aneurysm formation in Kawasaki disease in Han Chinese in Taiwan Sci Rep 5: 14762 [PMID: 26434682] |
Interaction Information:
Comment | Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis predominantly affecting infants and young children. Coronary artery aneurysm (CAA) is the major complication of KD. Chi-square tests for allelic and genotypic comparisons under the dominant model were performed to identify susceptibility gene loci associated with KD related CAA complications. A cluster of 35 genes that includes KCNQ5, PLCB1, PLCB4, and PLCL1 has been identified. |
Formal Description Interaction-ID: 110892 |
gene/protein affects_activity of phenotype coronary artery aneurysm |
Comment | Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis predominantly affecting infants and young children. Coronary artery aneurysm (CAA) is the major complication of KD. Chi-square tests for allelic and genotypic comparisons under the dominant model were performed to identify susceptibility gene loci associated with KD related CAA complications. A cluster of 35 genes that includes KCNQ5, PLCB1, PLCB4, and PLCL1 has been identified. |
Formal Description Interaction-ID: 110906 |
|
Comment | Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis predominantly affecting infants and young children. Coronary artery aneurysm (CAA) is the major complication of KD. Chi-square tests for allelic and genotypic comparisons under the dominant model were performed to identify susceptibility gene loci associated with KD related CAA complications. A cluster of 35 genes that includes KCNQ5, PLCB1, PLCB4, and PLCL1 has been identified. |
Formal Description Interaction-ID: 110908 |
gene/protein affects_activity of phenotype coronary artery aneurysm |
Comment | Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis predominantly affecting infants and young children. Coronary artery aneurysm (CAA) is the major complication of KD. Chi-square tests for allelic and genotypic comparisons under the dominant model were performed to identify susceptibility gene loci associated with KD related CAA complications. A cluster of 35 genes that includes KCNQ5, PLCB1, PLCB4, and PLCL1 has been identified. |
Formal Description Interaction-ID: 110909 |
|
Comment | Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis predominantly affecting infants and young children. Coronary artery aneurysm (CAA) is the major complication of KD. Chi-square tests for allelic and genotypic comparisons under the dominant model were performed to identify susceptibility gene loci associated with KD related CAA complications. A cluster of 35 genes that includes KCNQ5, PLCB1, PLCB4, and PLCL1 has been identified. |
Formal Description Interaction-ID: 110911 |
gene/protein affects_activity of phenotype coronary artery aneurysm |
Comment | Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis predominantly affecting infants and young children. Coronary artery aneurysm (CAA) is the major complication of KD. Chi-square tests for allelic and genotypic comparisons under the dominant model were performed to identify susceptibility gene loci associated with KD related CAA complications. A cluster of 35 genes that includes KCNQ5, PLCB1, PLCB4, and PLCL1 has been identified. |
Formal Description Interaction-ID: 110912 |
|
Comment | Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis predominantly affecting infants and young children. Coronary artery aneurysm (CAA) is the major complication of KD. Chi-square tests for allelic and genotypic comparisons under the dominant model were performed to identify susceptibility gene loci associated with KD related CAA complications. A cluster of 35 genes that includes KCNQ5, PLCB1, PLCB4, and PLCL1 has been identified. |
Formal Description Interaction-ID: 110946 |
|
Drugbank entries | Show/Hide entries for PLCL1 |
Comment | Kawasaki disease (KD) is an acute, inflammatory, and self-limited vasculitis predominantly affecting infants and young children. Coronary artery aneurysm (CAA) is the major complication of KD. Chi-square tests for allelic and genotypic comparisons under the dominant model were performed to identify susceptibility gene loci associated with KD related CAA complications. A cluster of 35 genes that includes KCNQ5, PLCB1, PLCB4, and PLCL1 has been identified. |
Formal Description Interaction-ID: 110947 |
|
Drugbank entries | Show/Hide entries for PLCL1 |
Comment | SNP rs6140791 was identified between PLCB4 and PLCB1. Plasma PLC levels were higher in patients with KD and CC+CG rs6140791 genotypes, and these genotypes were more prevalent in patients with KD who also had CAA. |
Formal Description Interaction-ID: 110949 |
increases_activity of phenotype coronary artery aneurysm |
Comment | Silencing KCNQ5, PLCB1, PLCB4, and PLCL1 inhibited the effect of lipopolysaccharide-induced endothelial cell inflammation with varying degrees of proinflammatory cytokine expression. |
Formal Description Interaction-ID: 115331 |
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Comment | Silencing KCNQ5, PLCB1, PLCB4, and PLCL1 inhibited the effect of lipopolysaccharide-induced endothelial cell inflammation with varying degrees of proinflammatory cytokine expression. |
Formal Description Interaction-ID: 115334 |
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Comment | Silencing KCNQ5, PLCB1, PLCB4, and PLCL1 inhibited the effect of lipopolysaccharide-induced endothelial cell inflammation with varying degrees of proinflammatory cytokine expression. |
Formal Description Interaction-ID: 115335 |
|
Comment | Silencing KCNQ5, PLCB1, PLCB4, and PLCL1 inhibited the effect of lipopolysaccharide-induced endothelial cell inflammation with varying degrees of proinflammatory cytokine expression. |
Formal Description Interaction-ID: 115336 |
|
Drugbank entries | Show/Hide entries for PLCL1 |