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SLC38A11

solute carrier family 38 member 11

HCNC Approved Symbol
SLC38A11 (HGNC:26836)
Genomic Coordinates
2:164,894,354 - 164,955,525 (2q24.3)
Synonyms
FLJ39822, AVT2
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 3 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SLC38A11 - Gene browser | 3billion