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SLC17A3

solute carrier family 17 member 3

HCNC Approved Symbol
SLC17A3 (HGNC:10931)
Genomic Coordinates
6:25,844,856 - 25,874,243 (6p22.2)
Synonyms
NPT4
Disease Associations
This gene is associated with the following 2 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC17A3 gene.

Frequently observed phenotypes

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

No Results
SLC17A3 - Gene browser | 3billion