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SNX21

sorting nexin family member 21

HCNC Approved Symbol
SNX21 (HGNC:16154)
Genomic Coordinates
20:45,833,799 - 45,843,276 (20q13.12)
Synonyms
dJ337O18.4, SNX-L, C20orf161
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.

SNX21 - Gene browser | 3billion