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MFSD2B

MFSD2 lysolipid transporter B, sphingolipid

HCNC Approved Symbol
MFSD2B (HGNC:37207)
Genomic Coordinates
2:24,010,085 - 24,026,775 (2p23.3)
Synonyms
SLC59A2
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 4 patients* with variant(s) predicted to be damaging.*2 of the patients have been diagnosed with a variant in another gene.

MFSD2B - Gene browser | 3billion