INT102336

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Context Info
Confidence 0.69
First Reported 2002
Last Reported 2003
Negated 0
Speculated 0
Reported most in Abstract
Documents 3
Total Number 6
Disease Relevance 2.54
Pain Relevance 0.49

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

cytoskeleton (Krit1) protein complex (Krit1)
Krit1 (Mus musculus)
Pain Link Frequency Relevance Heat
Spinal cord 6 91.28 High High
headache 10 88.48 High High
Central nervous system 2 84.80 Quite High
cva 20 83.52 Quite High
imagery 4 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Congenital Anomalies 12 95.28 Very High Very High Very High
Convulsion 8 92.72 High High
Ataxia 2 91.92 High High
Vascular Malformations 2 90.32 High High
Headache 10 88.48 High High
Stroke 2 86.72 High High
Cv General 3 Under Development 20 83.52 Quite High
Blister 2 74.96 Quite High
Nevus 2 74.56 Quite High
Syndrome 4 73.52 Quite High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
The mutation in exon 19 causes a premature stop codon (Q698X) predicted to produce a truncated Krev1 interaction-trapped 1 (KRIT1) protein.
Gene_expression (produce) of KRIT1
1) Confidence 0.69 Published 2002 Journal J. Neurol. Sci. Section Abstract Doc Link 11959162 Disease Relevance 1.17 Pain Relevance 0.18
The mutation in exon 19 causes a premature stop codon (Q698X) predicted to produce a truncated Krev1 interaction-trapped 1 (KRIT1) protein.
Gene_expression (produce) of interaction-trapped 1
2) Confidence 0.60 Published 2002 Journal J. Neurol. Sci. Section Abstract Doc Link 11959162 Disease Relevance 1.17 Pain Relevance 0.18
Patients in this family, harbouring the same mutation and chromosomes, are illustrative of the very variable clinical and radiological expression of a Krit1 mutation.
Gene_expression (expression) of Krit1
3) Confidence 0.47 Published 2003 Journal BMC Neurol Section Body Doc Link PMC184376 Disease Relevance 0 Pain Relevance 0
The report of a novel N-terminal region in Krit1 containing an NPXY motif interacting with icap1?
Gene_expression (region) of Krit1
4) Confidence 0.41 Published 2003 Journal BMC Neurol Section Body Doc Link PMC184376 Disease Relevance 0.06 Pain Relevance 0.07
Patients in this family, harbouring the same mutation, illustrate the very variable clinical and radiological expression of a Krit1 mutation.
Gene_expression (expression) of Krit1
5) Confidence 0.36 Published 2003 Journal BMC Neurol Section Abstract Doc Link PMC184376 Disease Relevance 0.07 Pain Relevance 0.03
Variable expression of cerebral cavernous malformations in carriers of a premature termination codon in exon 17 of the Krit1 gene

Background

Gene_expression (expression) of Krit1
6) Confidence 0.36 Published 2003 Journal BMC Neurol Section Title Doc Link PMC184376 Disease Relevance 0.08 Pain Relevance 0.04

General Comments

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