QuickView for GRIN3B;jsessionid=B71E1C0901675B8F1EF13731F1577521;jsessionid=5E7EAE1442C90CE392641C3E1C9CD838;jsessionid=05BF261DBB7ED6CC8A1EB33999EB4BE1 (gene)

Gene Symbol:

GRIN3B Homo sapiens

Full name:

glutamate ionotropic receptor NMDA type subunit 3B

Synonyms:

GluN3B, NR3B, glutamate receptor ionotropic, NMDA 3B, N-methyl-D-aspartate receptor subtype 3B, NMDA receptor subunit 3B, NMDA type glutamate receptor subunit NR3B, NMDAR3B, glutamate [NMDA] receptor subunit 3B, glutamate receptor, ionotropic, N-methyl-D-aspartate 3B

Genomic Location:

Chr 19: 951437-960723

Description:

The protein encoded by this gene is a subunit of an N-methyl-D-aspartate (NMDA) receptor. The encoded protein is found primarily in motor neurons, where it forms a heterotetramer with GRIN1 to create an excitatory glycine receptor. Variations in this gene have been proposed to be linked to schizophrenia.

The protein encoded by this gene is a subunit of an N-methyl-D-aspartate (NMDA) receptor. The encoded protein is found primarily in motor neurons, where it forms a heterotetramer with GRIN1 to create an excitatory glycine receptor. Variations in this gene have been proposed to be linked to schizophrenia.

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Orthologs:

Mus musculus ,  Rattus norvegicus ,  Macaca mulatta ,  Canis lupus familiaris ,  Danio rerio ,  Bos taurus

External Links:

Entrez Gene

Cytogenetic Map:

19p13.3

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