WB, ICC/IF, IHC, IHC-P, IPHost:
Hu, Primate, MonkeyApplications:
Applications: Flow, Flow-IC, IHC, IHC-P
Host: Mouse Monoclonal
Applications: WB, ELISA, PA
Mutations in Senataxin result in the neurodegenerative disorders Ataxia-Oculomotor Apraxia 2 (AOA2) and amyotrophic lateral sclerosis (ALS4). Senataxin bears an RNA/DNA helicase domain suggesting a role in DNA and RNA processing and has recently been found to be involved in the DNA damage response. Alternate names for Senataxin include SEN1 homolog, SETX, ALS4, KIAA0625, SCAR1, and AOA2.
|Product By Gene ID
- ALS4recessive, non-Friedreich type 1
Research Areas for Senataxin
Find related products by research area and learn more about each of the different research areas below.DNA Repair
Bioinformatics Tool for Senataxin
Discover related pathways, diseases and genes to Senataxin. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.