EcoDrugPlus

Glutamate Ionotropic Receptor Nmda Type Subunit 2a

Ensembl ID : ENSRBIG00000013802
Gene Symbol: GRIN2A
4 Cross references
227 Possible Orthologues:


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Glutamate Ionotropic Receptor Nmda Type Subunit 2b

Ensembl ID : ENSRBIG00000044052
Gene Symbol: GRIN2B
4 Cross references
330 Possible Orthologues:


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Glutamate Ionotropic Receptor Nmda Type Subunit 2c

Ensembl ID : ENSRBIG00000032178
Gene Symbol: GRIN2C
4 Cross references
244 Possible Orthologues:


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Glutamate Ionotropic Receptor Nmda Type Subunit 2d

Ensembl ID : ENSRBIG00000041836
Gene Symbol: GRIN2D
3 Cross references
278 Possible Orthologues:


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Glutamate Ionotropic Receptor Nmda Type Subunit 3a

Ensembl ID : ENSRBIG00000034056
Gene Symbol: GRIN3A
4 Cross references
245 Possible Orthologues:


Display Options: Drug type Mechanism of Action Route of Adminstration Status Therapeutic Area Therapeutic Indication

Glutamate Ionotropic Receptor Nmda Type Subunit 3b

Ensembl ID : ENSRBIG00000013801
Gene Symbol: GRIN3B
4 Cross references
286 Possible Orthologues:


Display Options: Drug type Mechanism of Action Route of Adminstration Status Therapeutic Area Therapeutic Indication

Glutamate Ionotropic Receptor Kainate Type Subunit 1

Ensembl ID : ENSRBIG00000030789
Gene Symbol: GRIK1
4 Cross references
302 Possible Orthologues:


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Glutamate Ionotropic Receptor Kainate Type Subunit 3

Ensembl ID : ENSRBIG00000036758
Gene Symbol: GRIK3
4 Cross references
256 Possible Orthologues:


Display Options: Drug type Mechanism of Action Route of Adminstration Status Therapeutic Area Therapeutic Indication

Glutamate Ionotropic Receptor Kainate Type Subunit 4

Ensembl ID : ENSRBIG00000028153
Gene Symbol: GRIK4
4 Cross references
261 Possible Orthologues:


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Glutamate Ionotropic Receptor Kainate Type Subunit 5

Ensembl ID : ENSRBIG00000039241
Gene Symbol: GRIK5
4 Cross references
302 Possible Orthologues:


Display Options: Drug type Mechanism of Action Route of Adminstration Status Therapeutic Area Therapeutic Indication

Glutamate Metabotropic Receptor 2

Ensembl ID : ENSRBIG00000030151
Gene Symbol: GRM2
4 Cross references
276 Possible Orthologues:


Display Options: Drug type Mechanism of Action Route of Adminstration Status Therapeutic Area Therapeutic Indication

Glutamate Metabotropic Receptor 3

Ensembl ID : ENSRBIG00000001135
Gene Symbol: GRM3
4 Cross references
215 Possible Orthologues:


Display Options: Drug type Mechanism of Action Route of Adminstration Status Therapeutic Area Therapeutic Indication

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PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains. Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).

PREMIER has received funding from the Innovative Medicines Initiative 2 Joint Undertaking (JU) under grant agreement No 875508. The JU receives support from the EU’s Horizon 2020 research and innovation programme and the European Federation of Pharmaceutical Industries and Associations (EFPIA). The views reflect only the authors’ perspective and the JU is not responsible for any use that may be made of the information this manuscript contains.

Elements of the website have been developed under projects PREMIER and the Biocenter Finland Drug Discovery and Chemical Biology network. CSC-IT is thanked for providing computational resources. Content of the website is provided without guarantee for correctness. Data has been collected and integrated from multiple public sources, for the largest: FDA, HUGO Gene Nomenclature Committee, ChEMBL, IUPHAR/BPS guide to pharmacology, Reactome, UniProt, and Ensembl. Credit is given to Ensembl for collecting species images (provided under public domain licences such as Wikimedia and NHGRI).