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SLC22A14

solute carrier family 22 member 14

HCNC Approved Symbol
SLC22A14 (HGNC:8495)
Genomic Coordinates
3:38,278,832 - 38,318,575 (3p22.2)
Synonyms
OCTL2, ORCTL4
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.

SLC22A14 - Gene browser | 3billion