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MFSD2A

MFSD2 lysolipid transporter A, lysophospholipid

HCNC Approved Symbol
MFSD2A (HGNC:25897)
Genomic Coordinates
1:39,955,145 - 39,969,956 (1p34.2)
Synonyms
FLJ14490, SLC59A1, MFSD2
Disease Associations
This gene is associated with the following 1 diseases in OMIM.
View More Disease Info
Disease NameOMIM IDInheritance
Neurodevelopmental disorder with progressive microcephaly, spasticity, and brain abnormalities
616486AR

Diagnosed Cases

0Patient

There are no patients diagnosed with a variant in the MFSD2A gene.

Frequently observed phenotypes

(Top 5 only, Patient count*)
*% of total patients presenting each phenotype is shown in parentheses.

No Results