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- Table of Contents
, No Gclids
pathway Info Card
Somal Translocation
Information about Somal Translocation: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Somal Translocation
Most recent studies have shown that Somal Translocation shares some biological mechanisms with axon-extension, axon-guidance, brain-development, cell-division, interphase, localization, locomotion, neurogenesis, neuron-migration, rna-interference, stem-cell-division.
Among the many pathways, these few ones have gauged particular interests from scientists studying Somal Translocation, and have been seen in publications frequently: axon-extension, axon-guidance, brain-development, cell-division, interphase, localization, locomotion, neurogenesis, neuron-migration, rna-interference, stem-cell-division
Quite a number of genes have been found to play important roles in Somal Translocation, such as CDK5, CP, DAB1, ELSPBP1, FGF8, FGFR1, GFAP, Hopx, MAZ, MICAL3, Oma1, PLXNA1, PLXNA2, PLXNB1, RELN, SLC7A5, Sema6a, TERF2IP. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this pathway. Plesae stay updated.
Diseases Related to Somal Translocation
This information is being compiled and will come in a future update
| brain diseases | classical lissencephaly | congenital abnormality |
| congenital neurologic anomalies | crest syndrome | lissencephaly |
| nervousness | proliferative inflammatory atrophy |