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SLC35F1

solute carrier family 35 member F1

HCNC Approved Symbol
SLC35F1 (HGNC:21483)
Genomic Coordinates
6:117,907,264 - 118,317,671 (6q22.2-q22.31)
Synonyms
dJ230I3.1, C6orf169
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.

SLC35F1 - Gene browser | 3billion