GRIN variants Database


Search for a GRIN variant

Indicate the Gene/s
ALL
GRIN1
GRIN2A
GRIN2B
GRIN2C
GRIN2D
GRIN3A
GRIN3B

Indicate the protein variant (optional):

p.

GRINdb stats (2025-03-24)

Missense
10691
Truncations
1118
Others
273
Total
12082

Disease-associated variants

Missense
582
Truncations
199
Others
12
Total
793

“GRIN database is a unified, integrated, updated, non-redundant and curated repository of all reported GRIN variants and related functional and clinical annotations.”


Note: Functional information and stratification of GRIN variants results from diverse experimental approaches, and rather than being a conclusive assessment, they correspond to the current view and interpretation performed by the authors of this database. GoF and Lof determinations have been made solely by the BCN group and were not provided by the source of the data/variant.

Partners & Collaborators

Institut d'Investigació Biomèdica de Bellvitge Universitat de Barcelona Universitat Central de Catalunya - Universitat de Vic Universitat Pompeu Fabra Hospital Sant Joan de Déu Instituto Carlos III Grinpatias Europa Asociación Española de Grinpatías Ayuntamiento de Concelho de Negreira Universitat Autònoma de Barcelona