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SNX32

sorting nexin 32

HCNC Approved Symbol
SNX32 (HGNC:26423)
Genomic Coordinates
: - (11q13.1)
Synonyms
FLJ30934, SNX6B
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 5 patients* with variant(s) predicted to be damaging.*4 of the patients have been diagnosed with a variant in another gene.

SNX32 - Gene browser | 3billion