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SLC16A8

solute carrier family 16 member 8

HCNC Approved Symbol
SLC16A8 (HGNC:16270)
Genomic Coordinates
22:38,078,137 - 38,084,184 (22q13.1)
Synonyms
MCT3, REMP
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.

SLC16A8 - Gene browser | 3billion