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SLC35G6

solute carrier family 35 member G6

HCNC Approved Symbol
SLC35G6 (HGNC:31351)
Genomic Coordinates
: - (17p13.1)
Synonyms
TMEM21B, AMAC1L3
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.

SLC35G6 - Gene browser | 3billion