INT232535

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Context Info
Confidence 0.58
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 2
Disease Relevance 1.49
Pain Relevance 0

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

endoplasmic reticulum (C1orf9)
C1orf9 (Homo sapiens)
Pain Link Frequency Relevance Heat
Inflammation 14 5.00 Very Low Very Low Very Low
Angina 8 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Acute Coronary Syndrome 64 99.28 Very High Very High Very High
Myocardial Infarction 124 98.00 Very High Very High Very High
Cancer 4 91.12 High High
Necrosis 2 90.64 High High
Coronary Artery Disease 76 5.00 Very Low Very Low Very Low
Metabolic Syndrome 16 5.00 Very Low Very Low Very Low
INFLAMMATION 14 5.00 Very Low Very Low Very Low
Aging 12 5.00 Very Low Very Low Very Low
Disease 12 5.00 Very Low Very Low Very Low
Atherosclerotic Plaque 8 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
However, the original C1orf9 SNP identified in the screen, rs2239816, is significantly associated in both GENECARD ACS (APL, p = 0.05) and CATHGEN MI samples (allele p = 0.04) and results in an amino acid change at position 11 (Pro11Ser).
Gene_expression (associated) of C1orf9 associated with acute coronary syndrome and myocardial infarction
1) Confidence 0.58 Published 2008 Journal BMC Med Genet Section Body Doc Link PMC2383879 Disease Relevance 0.74 Pain Relevance 0
Two SNPs, rs2239816 and rs1891586, reside within genes, chromosome 1 open reading frame 9 protein (C1orf9) and FAM5C, and the third within an intergenic region (rs1324713).
Gene_expression (reside) of C1orf9
2) Confidence 0.50 Published 2008 Journal BMC Med Genet Section Body Doc Link PMC2383879 Disease Relevance 0.75 Pain Relevance 0

General Comments

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