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


Search for a GRIN variant








(e.g. NM_000834.3:c.1657C>A, NC_000012.11:g.14018731C>A
or NM_000834.3:c.2360-2A>G)

GRINDB Information (2022-05-04)

Missense

4093

Truncations

345

Others

115


Total

4553

Disease-associated Unique Variants

Missense

334

Truncations

116

Others

19


Total

469



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 BellvitgeUniversitat de BarcelonaUniversitat Central de Catalunya - Universitat de Vic Universitat Pompeu FabraHospital Sant Joan de Déu

Instituto Carlos IIIGrinpatias EuropaAsociación Española de GrinpatíasAyuntamiento de Concelho de NegreiraUniversitat Autònoma de Barcelona