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SLC22A25

solute carrier family 22 member 25

HCNC Approved Symbol
SLC22A25 (HGNC:32935)
Genomic Coordinates
11:63,158,437 - 63,243,599 (11q12.3)
Synonyms
UST6, HIMTP, MGC120420
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 10 patients* with variant(s) predicted to be damaging.*5 of the patients have been diagnosed with a variant in another gene.

SLC22A25 - Gene browser | 3billion