EDG-5 Polyclonal Antibody, 100ul[BT-AP02832] Bottles Mutations in this gene cause

Mutations in this gene cause autosomal dominant nocturnal frontal lobe epilepsy type 4

UBTF (upstream binding transcription factor

MAP1A and MAP1B each consist of a heavy chain subunit and multiple light chain subunits

SLC30A9 (Solute Carrier Family 30 Member 9) is a Protein Coding gene

3'-diiodothyronine (T2)

EDG-5 Polyclonal Antibody, 100ul[BT-AP02832] Bottles Mutations in this gene causeS1PR2 encodes a member of the G protein coupled receptors, as well as the EDG family of proteins. The encoded protein (sphingosine 1 phosphate receptor 2) is a receptor for sphingosine 1 phosphate, which participates in cell proliferation, survival, and transcriptional activation. Defects in S1PR2 have been associated with congenital profound deafness.