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SLC17A2

solute carrier family 17 member 2

HCNC Approved Symbol
SLC17A2 (HGNC:10930)
Genomic Coordinates
6:25,912,754 - 25,930,691 (6p22.2)
Synonyms
NPT3
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

SLC17A2 - Gene browser | 3billion