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MFSD12

major facilitator superfamily domain containing 12

HCNC Approved Symbol
MFSD12 (HGNC:28299)
Genomic Coordinates
19:3,538,275 - 3,557,586 (19p13.3)
Synonyms
MGC20700, PP3501, SLC59B1, C19orf28
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.*1 of the patient has been diagnosed with a variant in another gene.

MFSD12 - Gene browser | 3billion