Applications: WB, IHC, IP
Host: Rabbit Polyclonal
Applications: WB, ELISA
Host: Mouse Monoclonal
Applications: WB, ELISA, PA
Applications: RNAi, RNAi SP
Defects in Retinoic acid-induced protein 1 (RAI1) are a cause of Smith-Magenis syndrome (SMS) [MIM:182290]. SMS is characterized by congenital mental retardation associated with development and growth delays. The RAI1 has also been associated with schizophrenia.
|Product By Gene ID
- Smith-Magenis syndrome chromosome region
- retinoic acid-induced protein 1
- retinoic acid induced 1
Bioinformatics Tool for RAI1
Discover related pathways, diseases and genes to RAI1. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.