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SLC17A9

solute carrier family 17 member 9

HCNC Approved Symbol
SLC17A9 (HGNC:16192)
Genomic Coordinates
20:62,952,709 - 62,969,585 (20q13.33)
Synonyms
FLJ23412, VNUT, C20orf59
Disease Associations
This gene is associated with the following 1 diseases in OMIM.

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the SLC17A9 gene.

Frequently observed phenotypes

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

No Results
SLC17A9 - Gene browser | 3billion