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SLC17A7

solute carrier family 17 member 7

HCNC Approved Symbol
SLC17A7 (HGNC:16704)
Genomic Coordinates
19:49,429,401 - 49,441,527 (19q13.33)
Synonyms
BNPI, VGLUT1
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 2 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SLC17A7 - Gene browser | 3billion