INT334577

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Context Info
Confidence 0.27
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 1.33
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.

KCNE1L (Homo sapiens)
Pain Link Frequency Relevance Heat
potassium channel 1 5.00 Very Low Very Low Very Low
Opioid receptor 1 1 5.00 Very Low Very Low Very Low
cocaine 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Syndrome 5 98.72 Very High Very High Very High
Alport Syndrome 1 98.32 Very High Very High Very High
Hearing Impairment 2 98.16 Very High Very High Very High
Intellectual Impairment 1 97.60 Very High Very High Very High
Elliptocytosis 1 95.92 Very High Very High Very High
Deafness 77 93.76 High High
Usher Syndrome 2 80.32 Quite High
Disease 85 41.12 Quite Low
Oxidative Phosphorylation Disease 1 5.00 Very Low Very Low Very Low
Nonsyndromic Deafness 1 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Similarly, KCNE1L has been associated by Piccini et al. [32] to AMME syndrome (Alport syndrome - mental retardation - midface hypoplasia - elliptocytosis) whose symptoms include, among others, hearing loss, and analogous situations are reported also for TIMM8A, involved in Mohr-Tranebjaerg syndrome [33] and Jensen syndrome [34], and ALMS1, involved in Alström syndrome [35].
KCNE1L Binding (associated) of associated with elliptocytosis, deafness, intellectual impairment, alport syndrome and syndrome
1) Confidence 0.27 Published 2010 Journal PLoS ONE Section Body Doc Link PMC2946934 Disease Relevance 1.33 Pain Relevance 0

General Comments

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