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SLC17A6

solute carrier family 17 member 6

HCNC Approved Symbol
SLC17A6 (HGNC:16703)
Genomic Coordinates
11:22,338,381 - 22,379,503 (11p14.3)
Synonyms
DNPI, VGLUT2
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 is 1 patient* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SLC17A6 - Gene browser | 3billion