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mfsd2aa


Official Full Name
MFSD2 lysolipid transporter A, lysophospholipid a
Organism
Danio rerio
Gene ID
492810
Background
Predicted to enable fatty acid transmembrane transporter activity and lysophospholipid:sodium symporter activity. Acts upstream of or within lysophospholipid transport and maintenance of blood-brain barrier. Predicted to be located in endoplasmic reticulum membrane. Predicted to be active in plasma membrane. Is expressed in axis; chondrocranium; nervous system; and polster. Used to study microcephaly. Human ortholog(s) of this gene implicated in primary autosomal recessive microcephaly 15. Orthologous to human MFSD2A (MFSD2 lysolipid transporter A, lysophospholipid). [provided by Alliance of Genome Resources, Feb 2025]
Synonyms
NLS1-A; mfsd2a; zgc:101615

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