GRIN2D wt Allele

**Semantic type:** Gene or Genome

**Definition:** Human GRIN2D wild-type allele is located in the vicinity of 19q13.33 and is approximately 51 kb in length. This allele, which encodes glutamate receptor ionotropic, NMDA 2D protein, plays a role in calcium and magnesium transport. Mutation of the gene is associated with developmental and epileptic encephalopathy 46.

**Synonyms:** - DEE46 - EB11 - EIEE46 - Estrogen Receptor Binding CpG Island Gene - GluN2D - Glutamate Ionotropic Receptor NMDA Type Subunit 2D wt Allele - Glutamate Receptor, Ionotropic, N-Methyl D-Aspartate 2D Gene - Glutamate Receptor, Ionotropic, N-Methyl-D-Aspartate, Subunit 2D Gene - N-Methyl-D-Aspartate Receptor Channel, Subunit Epsilon-4 Gene - NMDAR2D - NR2D