Mfsd2a Rabbit pAb

Enables fatty acid transmembrane transporter activity, lysophosphatidylcholine flippase activity, and lysophospholipid:sodium symporter activity. Involved in central nervous system development, lipid transport, and transcytosis. Acts upstream of or within several processes, including photoreceptor cell development, regulation of lipid metabolic process, and retina development in camera-type eye. Located in plasma membrane. Is integral component of plasma membrane. Is expressed in several structures, including alimentary system, central nervous system, genitourinary system, integumental system, and sensory organ. Human ortholog(s) of this gene implicated in primary autosomal recessive microcephaly 15. Orthologous to human MFSD2A (major facilitator superfamily domain containing 2A). Synonyma: NLS1, Mfsd2, 1700018O18Rik, Mfsd2a