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SNX18

sorting nexin 18

HCNC Approved Symbol
SNX18 (HGNC:19245)
Genomic Coordinates
: - (5q11.2)
Synonyms
SH3PX2, SH3PXD3B, SNAG1
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 7 patients* with variant(s) predicted to be damaging.*4 of the patients have been diagnosed with a variant in another gene.

SNX18 - Gene browser | 3billion