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SLC35D2

solute carrier family 35 member D2

HCNC Approved Symbol
SLC35D2 (HGNC:20799)
Genomic Coordinates
9:96,313,444 - 96,383,711 (9q22.32)
Synonyms
UGTrel8, SQV7L
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 3 patients* with variant(s) predicted to be damaging.*1 of the patient has been diagnosed with a variant in another gene.

SLC35D2 - Gene browser | 3billion