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GluD2

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Target not currently curated in GtoImmuPdb

Target id: 449

Nomenclature: GluD2

Family: Ionotropic glutamate receptors

Contents:

Gene and Protein Information Click here for help
Species TM P Loops AA Chromosomal Location Gene Symbol Gene Name Reference
Human 3 1 1007 4q22.1-q22.2 GRID2 glutamate ionotropic receptor delta type subunit 2
Mouse 3 1 1007 6 29.77 cM Grid2 glutamate receptor, ionotropic, delta 2
Rat 3 1 1007 4q31 Grid2 glutamate ionotropic receptor delta type subunit 2
Previous and Unofficial Names Click here for help
tpr | cpr | glutamate receptor
Database Links Click here for help
Alphafold O43424 (Hs), Q61625 (Mm), Q63226 (Rn)
ChEMBL Target CHEMBL4524129 (Hs)
Ensembl Gene ENSG00000152208 (Hs), ENSMUSG00000071424 (Mm), ENSRNOG00000006174 (Rn)
Entrez Gene 2895 (Hs), 14804 (Mm), 79220 (Rn)
Human Protein Atlas ENSG00000152208 (Hs)
KEGG Gene hsa:2895 (Hs), mmu:14804 (Mm), rno:79220 (Rn)
OMIM 602368 (Hs)
Orphanet ORPHA365089 (Hs)
Pharos O43424 (Hs)
RefSeq Nucleotide NM_001510 (Hs), NM_008167 (Mm), NM_024379 (Rn)
RefSeq Protein NP_001501 (Hs), NP_032193 (Mm), NP_077355 (Rn)
UniProtKB O43424 (Hs), Q61625 (Mm), Q63226 (Rn)
Wikipedia GRID2 (Hs)
Natural/Endogenous Ligands Click here for help
L-glutamic acid
Clinically-Relevant Mutations and Pathophysiology Click here for help
Disease:  Spinocerebellar ataxia, autosomal recessive 18; SCAR18
Synonyms: Autosomal recessive congenital cerebellar ataxia due to GRID2 deficiency [Orphanet: ORPHA363432]
OMIM: 616204
Orphanet: ORPHA363432

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