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Disease Info Card
Jerk Nystagmus
Information about Jerk Nystagmus: 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 Jerk Nystagmus
Most recent studies have shown that Jerk Nystagmus shares some biological mechanisms with achromatopsia, albinism, blind-vision, congenital-nystagmus, encephalitis, epilepsy, esotropia, hypoplasia, malnutrition, meniere-disease, migraine-disorders, neoplasms, nystagmus, ocular-motility-disorders, pendular-nystagmus, periodic-alternating-nystagmus, vertigo.
Among the many pathways, these few ones have gauged particular interests from scientists studying Jerk Nystagmus, and have been seen in publications frequently: Dehiscence, Pathogenesis, Reflex
Quite a number of genes have been found to play important roles in Jerk Nystagmus, such as ANPEP, BCHE, C2, C3, C6, CACNA1F, COX5A, DTL, FRMD7, HNRNPC, MB, PAG1, PRDX1, PSMA7, STATH, TNFSF14. 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.
Pathways Related to Jerk Nystagmus
This information is being compiled and will come in a future update
| Dehiscence | Pathogenesis | Reflex |