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SLC66A2

solute carrier family 66 member 2

HCNC Approved Symbol
SLC66A2 (HGNC:26188)
Genomic Coordinates
: - (18q23)
Synonyms
FLJ22378, PQLC1
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 2 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

SLC66A2 - Gene browser | 3billion