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SNX22

sorting nexin 22

HCNC Approved Symbol
SNX22 (HGNC:16315)
Genomic Coordinates
: - (15q22.31)
Synonyms
FLJ13952
Disease Associations
Currently, this gene is not associated with any human disease in OMIM.

Diagnosed Cases

There are no diagnosed cases at this time.
There are no patients* with variants predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

SNX22 - Gene browser | 3billion