INT329074

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Context Info
Confidence 0.66
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.37
Pain Relevance 0.08

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

protein modification process (Pcmtd2) methyltransferase activity (Pcmtd2) molecular_function (Pcmtd2)
cellular_component (Pcmtd2) biological_process (Pcmtd2) cytoplasm (Pcmtd2)
Pcmtd2 (Mus musculus)
Pain Link Frequency Relevance Heat
Central nervous system 1 86.32 High High
Neuronal excitability 1 79.92 Quite High
Pain 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Convulsion 16 82.24 Quite High
Epilepsy 6 76.04 Quite High
Anxiety Disorder 2 72.92 Quite High
Targeted Disruption 1 71.76 Quite High
Frontal Lobe Epilepsy 1 49.28 Quite Low
Benign Neonatal Epilepsy 1 46.80 Quite Low
Neurological Disease 1 46.16 Quite Low
Cognitive Disorder 3 43.36 Quite Low
Partial Seizures 2 34.16 Quite Low
Fever 2 25.64 Quite Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The smallest 20q13.33 microdeletion, report by Kroepfl and colleagues [8], is a subtelomere microdeletion encompassing only two genes, myelin transcription factor 1 (MYTI) and protein-L-isoaspartate (D-aspartate) O-methyltransferase domain containing 2 (PCMTD2) (Figure 1).
Transcription (transcription) of PCMTD2
1) Confidence 0.66 Published 2010 Journal PLoS ONE Section Body Doc Link PMC2929201 Disease Relevance 0.37 Pain Relevance 0.08

General Comments

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