INT237354

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Context Info
Confidence 0.40
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 2
Disease Relevance 1.22
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.

cytoplasm (DNM2, Bin1) nucleus (DNM2, Bin1) cell differentiation (Bin1)
enzyme binding (DNM2) GTPase activity (DNM2) cytosol (DNM2)
DNM2 (Homo sapiens)
Bin1 (Mus musculus)
Pain Link Frequency Relevance Heat
Inflammation 4 5.00 Very Low Very Low Very Low
ketamine 2 5.00 Very Low Very Low Very Low
anesthesia 2 5.00 Very Low Very Low Very Low
sodium channel 2 5.00 Very Low Very Low Very Low
Sciatic nerve 2 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Congenital Structural Myopathies 34 97.60 Very High Very High Very High
Muscle Hypotonia 2 91.20 High High
Muscle Weakness 8 90.08 High High
Death 4 28.16 Quite Low
Cytomegalovirus Infection 26 5.00 Very Low Very Low Very Low
Disease 10 5.00 Very Low Very Low Very Low
Muscle Disease 10 5.00 Very Low Very Low Very Low
Charcot Marie Tooth Disease 8 5.00 Very Low Very Low Very Low
Demyelinating Disease 4 5.00 Very Low Very Low Very Low
INFLAMMATION 4 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Missense mutations in DNM2 (dynamin 2) are found in most patients in the autosomal dominant form (4,5), and recently, mutations in amphiphysin 2/Bin1, a dynamin 2 interactor, have been found in some patients with autosomal recessive CNM (6).
dynamin 2 Binding (interactor) of Bin1 associated with congenital structural myopathies
1) Confidence 0.40 Published 2008 Journal Human Molecular Genetics Section Body Doc Link PMC2441725 Disease Relevance 0.61 Pain Relevance 0
Missense mutations in DNM2 (dynamin 2) are found in most patients in the autosomal dominant form (4,5), and recently, mutations in amphiphysin 2/Bin1, a dynamin 2 interactor, have been found in some patients with autosomal recessive CNM (6).
dynamin 2 Binding (interactor) of amphiphysin 2 associated with congenital structural myopathies
2) Confidence 0.40 Published 2008 Journal Human Molecular Genetics Section Body Doc Link PMC2441725 Disease Relevance 0.61 Pain Relevance 0

General Comments

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