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SLC22A31

solute carrier family 22 member 31

HCNC Approved Symbol
SLC22A31 (HGNC:27091)
Genomic Coordinates
: - (16q24.3)
Synonyms
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 4 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SLC22A31 - Gene browser | 3billion