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SLC17A8

solute carrier family 17 member 8

HCNC Approved Symbol
SLC17A8 (HGNC:20151)
Genomic Coordinates
12:100,357,074 - 100,422,055 (12q23.1)
Synonyms
VGLUT3, DFNA25
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

2Patients

In total, 2 patients were diagnosed with a variant in the SLC17A8 gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results
SLC17A8 - Gene browser | 3billion