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SLC22A13

solute carrier family 22 member 13

HCNC Approved Symbol
SLC22A13 (HGNC:8494)
Genomic Coordinates
3:38,265,812 - 38,278,757 (3p22.2)
Synonyms
OCTL1, OCTL3, OAT10, ORCTL3
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 is 1 patient* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SLC22A13 - Gene browser | 3billion