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SLC16A13

solute carrier family 16 member 13

HCNC Approved Symbol
SLC16A13 (HGNC:31037)
Genomic Coordinates
: - (17p13.1)
Synonyms
MCT13
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

SLC16A13 - Gene browser | 3billion