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SLC22A23

solute carrier family 22 member 23

HCNC Approved Symbol
SLC22A23 (HGNC:21106)
Genomic Coordinates
6:3,268,973 - 3,457,050 (6p25.2)
Synonyms
FLJ22174, C6orf85
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 20 patients* with variant(s) predicted to be damaging.*8 of the patients have been diagnosed with a variant in another gene.

SLC22A23 - Gene browser | 3billion