INT231206

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Context Info
Confidence 0.22
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 2
Total Number 3
Disease Relevance 1.04
Pain Relevance 0.24

This is a graph with borders and nodes. Maybe there is an Imagemap used so the nodes may be linking to some Pages.

plasma membrane (KCNH2, KCNQ1) transmembrane transport (KCNH2, KCNQ1) nuclear envelope (KCNH2)
cytoplasm (KCNH2)
KCNH2 (Homo sapiens)
KCNQ1 (Homo sapiens)
Pain Link Frequency Relevance Heat
sodium channel 31 96.00 Very High Very High Very High
potassium channel 3 72.72 Quite High
Action potential 10 27.16 Quite Low
tetrodotoxin 2 26.64 Quite Low
lidocaine 2 25.28 Quite Low
beta blocker 3 23.68 Low Low
imagery 2 21.20 Low Low
Calcium channel 3 5.00 Very Low Very Low Very Low
fibrosis 1 5.00 Very Low Very Low Very Low
Inflammation 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Dilated Cardiomyopathy 32 99.76 Very High Very High Very High
Congenital Anomalies 4 98.80 Very High Very High Very High
Syndrome 45 93.20 High High
Disease 25 89.52 High High
Arrhythmogenic Right Ventricular Dysplasia 10 68.20 Quite High
Sudden Death 16 58.40 Quite High
Syncope 13 57.84 Quite High
Arrhythmias 2 Under Development 25 50.00 Quite Low
Bundle-branch Block 15 36.28 Quite Low
Malignant Neoplastic Disease 3 27.20 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Similar analysis excluded possible mutations that would lead to amino acid changes in KCNQ1, HERG, and LAMIN A/C commonly associated with LQT1, LQT2, and DCM with conduction disorders on earlier occasions:11–13 we did not find new mutations that would lead to amino acid changes.
LQT2 Binding (associated) of KCNQ1 associated with dilated cardiomyopathy
1) Confidence 0.22 Published 2008 Journal Europace Section Body Doc Link PMC2573028 Disease Relevance 0.33 Pain Relevance 0.08
Similar analysis excluded possible mutations that would lead to amino acid changes in KCNQ1, HERG, and LAMIN A/C commonly associated with LQT1, LQT2, and DCM with conduction disorders on earlier occasions:11–13 we did not find new mutations that would lead to amino acid changes.
HERG Binding (associated) of LQT1 associated with dilated cardiomyopathy
2) Confidence 0.22 Published 2008 Journal Europace Section Body Doc Link PMC2573028 Disease Relevance 0.28 Pain Relevance 0.08
LQT2 is characterized by higher penetrance and severity than LQT1, especially for females [13].
LQT2 Binding (characterized) of LQT1
3) Confidence 0.16 Published 2008 Journal Indian Pacing and Electrophysiology Journal Section Body Doc Link PMC2363724 Disease Relevance 0.42 Pain Relevance 0.07

General Comments

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