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GRIN3B

glutamate ionotropic receptor NMDA type subunit 3B

HCNC Approved Symbol
GRIN3B (HGNC:16768)
Genomic Coordinates
19:1,000,419 - 1,009,732 (19p13.3)
Synonyms
GluN3B
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
However, there are 6 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

GRIN3B - Gene browser | 3billion