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SLC7A11

solute carrier family 7 member 11

HCNC Approved Symbol
SLC7A11 (HGNC:11059)
Genomic Coordinates
4:138,164,097 - 138,312,671 (4q28.3)
Synonyms
xCT
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 2 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

SLC7A11 - Gene browser | 3billion