INT229081

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Context Info
Confidence 0.62
First Reported 2008
Last Reported 2010
Negated 0
Speculated 0
Reported most in Body
Documents 2
Total Number 2
Disease Relevance 0.39
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.

transport (MYO5A) Golgi apparatus (MYO5A) cytoplasm (MYO5A)
MYO5A (Homo sapiens)
Pain Link Frequency Relevance Heat
melanocortin 1 receptor 6 5.00 Very Low Very Low Very Low
Glutamate receptor 1 5.00 Very Low Very Low Very Low
anesthesia 1 5.00 Very Low Very Low Very Low
Pain 1 5.00 Very Low Very Low Very Low
Disease Link Frequency Relevance Heat
Hypopigmentation 6 95.44 Very High Very High Very High
Li-fraumeni Syndrome 35 78.12 Quite High
Syndrome 22 13.00 Low Low
Neurologic Manifestations 2 7.68 Low Low
Disease 6 5.00 Very Low Very Low Very Low
Rickets 2 5.00 Very Low Very Low Very Low
Immunodeficiency 2 5.00 Very Low Very Low Very Low
Epilepsy 2 5.00 Very Low Very Low Very Low
Microphthalmia 2 5.00 Very Low Very Low Very Low
Congenital Anomalies 2 5.00 Very Low Very Low Very Low

Sentences Mentioned In

Key: Protein Mutation Event Anatomy Negation Speculation Pain term Disease term
Only 10 Ensembl Gene Predictions fell within this region, including MYO5A, but not RAB27A (UCSC Genome Browser [9]).


Gene_expression (fell) of MYO5A
1) Confidence 0.62 Published 2010 Journal PLoS Genetics Section Body Doc Link PMC2855325 Disease Relevance 0.15 Pain Relevance 0
The rs4776053 allele was in the myosin VA gene found only in the Caucasoid group, and the other alleles of the combination, rs2311843 and rs1800404, were both in the oculocutaneous albinism II gene, found in both groups.
Gene_expression (found) of myosin VA gene associated with hypopigmentation
2) Confidence 0.43 Published 2008 Journal International Journal of Biological Sciences Section Body Doc Link PMC2288787 Disease Relevance 0.23 Pain Relevance 0

General Comments

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