INT142004

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Context Info
Confidence 0.00
First Reported 2007
Last Reported 2007
Negated 0
Speculated 0
Reported most in Abstract
Documents 1
Total Number 1
Disease Relevance 1.02
Pain Relevance 0.26

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

cell death (Cacna1a, TGM6) plasma membrane (Cacna1a) nucleus (Cacna1a)
transferase activity, transferring acyl groups (TGM6) neurological system process (Cacna1a) transmembrane transport (Cacna1a)
Cacna1a (Rattus norvegicus)
TGM6 (Homo sapiens)
Pain Link Frequency Relevance Heat
Migraine 1 99.82 Very High Very High Very High
Calcium channel 1 97.96 Very High Very High Very High
headache 2 60.56 Quite High
Disease Link Frequency Relevance Heat
Ataxia 5 100.00 Very High Very High Very High
Spinocerebellar Ataxia Type 2 4 100.00 Very High Very High Very High
Migraine With Aura 1 99.82 Very High Very High Very High
Vertigo 2 61.44 Quite High
Headache 2 60.56 Quite High
Frailty 1 37.36 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Familial hemiplegic migraine type 1, spinocerebellar ataxia type 6 (SCA6) and episodic ataxia type 2 (EA2) are allelic disorders associated with mutations in the CACNA1A gene, which encodes the alpha1 subunit of the P/Q-type calcium channel (Ca(V)2.1).
CACNA1A gene Binding (associated) of spinocerebellar ataxia type 6 associated with ataxia, migraine with aura, calcium channel, migraine and spinocerebellar ataxia type 2
1) Confidence 0.00 Published 2007 Journal J. Neurol. Sci. Section Abstract Doc Link 17292920 Disease Relevance 1.02 Pain Relevance 0.26

General Comments

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