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Disease Info Card
Hyperexplexia
Information about Hyperexplexia: 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 Hyperexplexia
Most recent studies have shown that Hyperexplexia shares some biological mechanisms with apnea, congenital-stiff-person-syndrome, encephalopathies, epilepsy, movement-disorders, muscle-hypertonia, muscle-rigidity, myoclonus, myoclonus-nocturnal, nervous-system-disorder, nervousness, reflex-abnormal, spasm, stiff-person-syndrome, sudden-infant-death-syndrome.
Among the many pathways, these few ones have gauged particular interests from scientists studying Hyperexplexia, and have been seen in publications frequently: Cell Division, Fertilization, Gephyrin Clustering, Glycine Transport, Habituation, Interphase, Localization, Mating, Myelination, Neuromuscular Junction Development, Pathogenesis, Prepulse Inhibition, Receptor Clustering, Reflex, Righting Reflex, Secretion, Sensory Processing, Startle Response, Synaptic Transmission, Transport
Quite a number of genes have been found to play important roles in Hyperexplexia, such as ABCB6, ARHGEF9, CFTR, CHAT, CHRM1, EPHA3, GLRA1, GLRB, GPHN, HOXD13, MTSS1, PRNP, QPCT, SCN9A, SLC32A1, SLC6A2, SLC6A5. 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 disease. Plesae stay updated.