Applications: WB, ELISA
Host: Mouse Monoclonal
WB, ELISA, PA, AP
The ENAM gene encodes from enamelin which is 1,142 amino acids long at 128 kDA and functions in the mineralization and structural organization of enamel. Defects in ENAM lead to amelogenesis imperfect type 1B and 1C. ENAM interacts with genes MFAP5, AHSG, SEP15, C11orf68, and TMEM66. ENAM has also been linked to cleft lip/palate, kidney disease, hepatitis c, dentin dysplasia, amelogenesis imperfecta, and craniopharyngioma.
|Product By Gene ID
- amelogenesis imperfecta 2, hypocalcification (autosomal dominant)
Bioinformatics Tool for Enamelin
Discover related pathways, diseases and genes to Enamelin. Need help? Read the Bioinformatics Tool Guide
for instructions on using this tool.