GRIN2A

NMDA receptor subunit GluN2A

AF-Q12879-F1 · v6 · Human reference sequence 1–1,464

Predicted backbone

Drag to rotate, or use the arrow keys on the model. Select a residue below to inspect its pLDDT.

The original model and trace download are linked below.

≥9070–<9050–<70<50

Research links

Schizophrenia

Rare variant study

A large schizophrenia exome study implicates GRIN2A through a gene-level burden of rare damaging coding variants.

Singh et al., 2022

Provenance and confidence

AlphaFold DB prediction by Google DeepMind and EMBL-EBI. The viewer draws a Cα trace derived from the RCSB BinaryCIF copy. We matched the release, residue sequence and mean pLDDT against AlphaFold DB.

Model: AF-Q12879-F1 · v6
Retrieved: 2026-11-14
Mean pLDDT: 60.85 / 100
Residues by band: ≥90 · 275 / 70–<90 · 429 / 50–<70 · 126 / <50 · 634
Coordinate SHA-256: d1be5a768910792cd0fc1296eda4a1f59aa9a0484e6d6320d1d3c6a08f2ecc56
License: CC BY 4.0

AlphaFold entry and PAE viewer RCSB model BinaryCIF coordinates Trace JSON

Varadi et al. · AlphaFold DB