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Disease Info Card
Cataplexy
Information about Cataplexy: 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 Cataplexy
Most recent studies have shown that Cataplexy shares some biological mechanisms with apnea, autoimmune-reaction, cataplexy-and-narcolepsy, depressive-disorder, disorders-of-excessive-somnolence, epilepsy, excessive-daytime-somnolence, hallucinations, hypersomnolence-idiopathic, hypnagogic-hallucination, narcolepsy, narcolepsy-without-cataplexy, nervous-system-disorder, nervousness, primary-hypersomnia, sleep-apnea-obstructive, sleep-apnea-syndromes, sleep-attacks, sleep-disorders, sleep-paralysis.
Among the many pathways, these few ones have gauged particular interests from scientists studying Cataplexy, and have been seen in publications frequently: Aging, Cell Death, Cholesterol Esterification, Circadian Rhythm, Cognition, Energy Homeostasis, Excretion, Feeding Behavior, Hormone Secretion, Hypersensitivity, Immune Response, Innervation, Lipid Storage, Localization, Locomotion, Pathogenesis, Reflex, Secretion, Translation, Transport
Quite a number of genes have been found to play important roles in Cataplexy, such as CD200R1, CHN1, COMT, CSF2, CTNNBL1, DIO2, HCRT, HCRTR2, HLA-DRB1, HLA-DRB4, HLA-DRB5, LAMC2, LIFR, NPC1, NPC2, PNPLA6, REM1. 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.