Applications: WB, ELISA(Cap)
Host: Mouse Monoclonal
WB, ELISA, IHC, IHC-PHost:
Applications: Binding Activity
EDA-A1 and EDA-A2 are two isoforms of ectodysplasin that are encoded by the anhidrotic ectodermal dysplasia (EDA) gene. Mutations in EDA give rise to a clinical syndrome characterized by loss of hair, sweat glands, and teeth. The protein encoded by this gene specifically binds to EDA-A2 isoform. This protein is a type III transmembrane protein of the TNFR (tumor necrosis factor receptor) superfamily, and contains 3 cysteine-rich repeats and a single transmembrane domain but lacks an N-terminal signal peptide. Multiple alternatively spliced transcript variants have been found for this gene, but some variants lack sufficient support.
|Product By Gene ID
- EDA-A2 receptor
- EDAA2Rtumor necrosis factor receptor superfamily member XEDAR
- XEDARTNFRSF27tumor necrosis factor receptor superfamily member 27
- X-linked ectodysplasin-A2 receptor
- ectodysplasin A2 receptor
Bioinformatics Tool for EDA2R/TNFRSF27/XEDAR
Discover related pathways, diseases and genes to EDA2R/TNFRSF27/XEDAR. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.