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MFSD6L

major facilitator superfamily domain containing 6 like

HCNC Approved Symbol
MFSD6L (HGNC:26656)
Genomic Coordinates
: - (17p13.1)
Synonyms
FLJ35773
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 is 1 patient* with variant(s) predicted to be damaging.* None of the patients have been diagnosed with a variant in another gene.

MFSD6L - Gene browser | 3billion