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SLC26A7

solute carrier family 26 member 7

HCNC Approved Symbol
SLC26A7 (HGNC:14467)
Genomic Coordinates
8:91,209,496 - 91,398,155 (8q21.3)
Synonyms
SUT2
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.* None of the patients have been diagnosed with a variant in another gene.

SLC26A7 - Gene browser | 3billion