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SLC2A13

solute carrier family 2 member 13

HCNC Approved Symbol
SLC2A13 (HGNC:15956)
Genomic Coordinates
12:39,755,025 - 40,106,081 (12q12)
Synonyms
HMIT
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 19 patients* with variant(s) predicted to be damaging.*15 of the patients have been diagnosed with a variant in another gene.

SLC2A13 - Gene browser | 3billion