INT277258

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Context Info
Confidence 0.81
First Reported 2009
Last Reported 2009
Negated 0
Speculated 1
Reported most in Body
Documents 1
Total Number 5
Disease Relevance 3.59
Pain Relevance 0.04

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

nucleus (Satb2) DNA binding (Satb2) cytoplasm (Satb2)
Anatomy Link Frequency
jaw 1
tooth 1
Satb2 (Mus musculus)
Pain Link Frequency Relevance Heat
imagery 5 76.28 Quite High
tolerance 5 5.00 Very Low Very Low Very Low
Pain 5 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Autism 10 99.80 Very High Very High Very High
Tooth Abnormalities 20 99.78 Very High Very High Very High
Intellectual Impairment 65 99.14 Very High Very High Very High
Cleft Palate 70 97.00 Very High Very High Very High
Syndrome 80 96.36 Very High Very High Very High
Diastema 5 90.72 High High
Malocclusion 10 90.16 High High
Pica 5 89.64 High High
Aggression 25 89.24 High High
Congenital Anomalies 35 87.60 High High

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Additionally, one individual with a balanced translocation disrupting SATB2 had autism spectrum disorder [9].
Localization (translocation) of SATB2 associated with autism
1) Confidence 0.81 Published 2009 Journal PLoS ONE Section Body Doc Link PMC2719055 Disease Relevance 0.59 Pain Relevance 0.04
These relatives were not available for testing to determine their SATB2 genotype.
Spec (determine) Localization (genotype) of SATB2
2) Confidence 0.75 Published 2009 Journal PLoS ONE Section Body Doc Link PMC2719055 Disease Relevance 0.77 Pain Relevance 0
Our results suggest that deletion of SATB2 is responsible for several of the clinical features associated with 2q32q33 microdeletion syndrome.



Localization (deletion) of SATB2 associated with syndrome
3) Confidence 0.75 Published 2009 Journal PLoS ONE Section Abstract Doc Link PMC2719055 Disease Relevance 0.61 Pain Relevance 0
The role of SATB2 in tooth and jaw development is supported by the identification of a de novo SATB2 mutation in a male with profound mental retardation and jaw and tooth abnormalities [7] and a translocation interrupting SATB2 in an individual with Robin sequence [8].
Localization (translocation) of SATB2 in tooth associated with tooth abnormalities and intellectual impairment
4) Confidence 0.71 Published 2009 Journal PLoS ONE Section Body Doc Link PMC2719055 Disease Relevance 0.81 Pain Relevance 0
The role of SATB2 in tooth and jaw development is supported by the identification of a de novo SATB2 mutation in a male with profound mental retardation and jaw and tooth abnormalities [7] and a translocation interrupting SATB2 in an individual with Robin sequence [8].
Localization (translocation) of SATB2 in jaw associated with tooth abnormalities and intellectual impairment
5) Confidence 0.24 Published 2009 Journal PLoS ONE Section Body Doc Link PMC2719055 Disease Relevance 0.81 Pain Relevance 0

General Comments

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