INT334578

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Context Info
Confidence 0.21
First Reported 2010
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.83
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.

plasma membrane (SLC26A4) transmembrane transport (SLC26A4)
Anatomy Link Frequency
inner ear 1
SLC26A4 (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
Deafness 77 99.36 Very High Very High Very High
Syndrome 5 98.12 Very High Very High Very High
Sensorineural Hearing Loss 1 84.68 Quite High
Oxidative Phosphorylation Disease 1 80.08 Quite High
Nonsyndromic Deafness 1 51.44 Quite High
Disease 85 11.68 Low Low
Usher Syndrome 2 5.00 Very Low Very Low Very Low
Hearing Impairment 2 5.00 Very Low Very Low Very Low
Elliptocytosis 1 5.00 Very Low Very Low Very Low
Alport Syndrome 1 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
For instance, SLC26A4, associated with autosomal recessive NSHL [4] and Pendred syndrome, is a gene coding for pendrin, a chloride/iodide transporter; COCH, responsible for autosomal dominant non syndromic post-lingual with a progressive onset in adulthood [5], encodes for cochlin, a component of the extracellular matrix of the inner ear; POU3F4, responsible for an X-linked non syndromic progressive and profound sensorineural hearing loss [6], encodes for a transcription factor; while WFS1 associated with autosomal recessive Wolfram syndrome and autosomal dominant low frequency NSHL [7], [8], is a gene coding for the glycoprotein wolframin.
SLC26A4 Binding (associated) of in inner ear associated with oxidative phosphorylation disease, deafness, syndrome and sensorineural hearing loss
1) Confidence 0.21 Published 2010 Journal PLoS ONE Section Body Doc Link PMC2946934 Disease Relevance 0.83 Pain Relevance 0

General Comments

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