subtype 2B (NMDAR2B or NR2B), is a protein that in humans is encoded by the GRIN2B gene. N-methyl-D-aspartate (NMDA) receptors are a class of ionotropic glutamate...
16 KB (1,905 words) - 18:16, 16 May 2024
GRIN2B-related neurodevelopmental disorder is a rare neurodevelopmental disorder which is characterized by developmental delays and intellectual disabilities...
6 KB (324 words) - 22:30, 26 July 2022
GluK4/GRIK4; GluK5/GRIK5; NMDA receptors: GluN1/GRIN1; GluN2A/GRIN2A; GluN2B/GRIN2B; GluN2C/GRIN2C; GluN2D/GRIN2D; GluN3A/GRIN3A; GluN3B/GRIN3B; Traynelis SF...
5 KB (433 words) - 06:16, 15 October 2023
NMDA receptor are encoded by GRIN genes: GRIN1 codes for GluN1; GRIN2A, GRIN2B, GRIN2C, and GRIN2D code for GluN2 A to D; GRIN3A and GRIN3B code for GluN3A...
8 KB (718 words) - 07:00, 15 April 2024
more than one splice variant. GluN1 – GRIN1 GluN2 GluN2A – GRIN2A GluN2B – GRIN2B GluN2C – GRIN2C GluN2D – GRIN2D GluN3 GluN3A – GRIN3A GluN3B – GRIN3B The...
107 KB (12,051 words) - 17:52, 31 May 2024
ETFA, ETFB, ETFDH recessive GRACILE syndrome BCS1L GRIN2B-related neurodevelopmental disorder GRIN2B Griscelli syndrome MYO5A, RAB27A, MLPH Gustavson syndrome...
42 KB (969 words) - 16:02, 3 April 2024
GRINL1B GLUN1, NMDA-R1, NR1, GluRξ1 GluN2A GluN2B GluN2C GluN2D GRIN2A GRIN2B GRIN2C GRIN2D GLUN2A, NMDA-R2A, NR2A, GluRε1 GLUN2B, NMDA-R2B, NR2B, hNR3...
29 KB (2,597 words) - 03:43, 7 April 2024
technique.[unreliable source?] In 2006 the glutamate receptor subunit gene GRIN2B (responsible for key functions in memory and learning) was associated with...
63 KB (6,876 words) - 18:10, 26 April 2024
DLGAP1 DLGAP2 DYNLL1 DYNLL2 ERBB4 EXOC4 FYN FZD7 GRIK1 GRIK2 GRIK5 GRIN2A GRIN2B GRIN2C HER2/neu HGS KCNA2 KCNA4 KCNA5 KCNJ12 Kir2.1 LGI1 LRP1 LRP2 NLGN1...
23 KB (2,725 words) - 03:04, 19 December 2023
Another gene that has been associated with this condition is GRIN1 and GRIN2B. The effects of PMG can be either focal or widespread. Although both can...
28 KB (3,206 words) - 16:55, 28 February 2024