INT272015

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Context Info
Confidence 0.18
First Reported 2008
Last Reported 2008
Negated 0
Speculated 0
Reported most in Body
Documents 1
Total Number 1
Disease Relevance 0.65
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.

cytosol (TSC1) Golgi apparatus (Pkd1) plasma membrane (Pkd1)
nucleus (Pkd1) embryo development (TSC1) cilium (Pkd1)
Anatomy Link Frequency
kidney 2
Pkd1 (Mus musculus)
TSC1 (Homo sapiens)
Pain Link Frequency Relevance Heat
cerebral cortex 1 5.00 Very Low Very Low Very Low
transdermal 1 5.00 Very Low Very Low Very Low
adenocard 1 5.00 Very Low Very Low Very Low
Angina 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Disease 21 100.00 Very High Very High Very High
Autosomal Dominant Polycystic Kidney 1 97.86 Very High Very High Very High
Syndrome 2 91.28 High High
Tuberous Sclerosis 11 50.00 Quite Low
Cancer 20 5.00 Very Low Very Low Very Low
Angiomyolipoma 12 5.00 Very Low Very Low Very Low
Lymphangioleiomyomatosis 11 5.00 Very Low Very Low Very Low
Convulsion 9 5.00 Very Low Very Low Very Low
Hamartoma 8 5.00 Very Low Very Low Very Low
Anaplastic Astrocytoma 6 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Major genes for TSC and autosomal dominant polycystic kidney disease (PKD), TSC2 and PKD1, respectively, lie adjacent to each other at chromosome 16p3.3, suggesting a role for PKD1 in the etiology of renal cystic disease in TSC.
PKD1 Positive_regulation (role) of Localization (disease) of TSC in kidney associated with autosomal dominant polycystic kidney and disease
1) Confidence 0.18 Published 2008 Journal Current Genomics Section Body Doc Link PMC2691673 Disease Relevance 0.65 Pain Relevance 0

General Comments

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