Mfsd2a - MFSD2 lysolipid transporter A, lysophospholipid Gene

Rattus norvegicus

Also known as Mfsd2; RGD1310174

Gene ID: 298504 | Gene type: protein coding

About Mfsd2a

Summary

Predicted to enable lysophosphatidylcholine flippase activity; lysophospholipid:sodium symporter activity; and oleate transmembrane transporter activity. Predicted to be involved in central nervous system development; lipid transport; and transcytosis. Predicted to act upstream of or within several processes, including photoreceptor cell development; regulation of lipid metabolic process; and retina development in camera-type eye. Predicted to be located in plasma membrane. Predicted to be integral component of plasma membrane. Human ortholog(s) of this gene implicated in primary autosomal recessive microcephaly 15. Orthologous to human MFSD2A (major facilitator superfamily domain containing 2A). [provided by Alliance of Genome Resources, Apr 2022]

Mfsd2a Products(1)

mRNA	Protein	Name
NM_001106683.1	NP_001100153.1	sodium-dependent lysophosphatidylcholine symporter 1

Protein Preferred Names

Protein Names

sodium-dependent lysophosphatidylcholine symporter 1

major facilitator superfamily domain containing 2

major facilitator superfamily domain containing 2A

Related Agents

Pre-clinical Phase

Bioactive Molecules (2)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS08391	MFSD2A Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown
HY-164994	LysoPC (18:4(6Z,9Z,12Z,15Z))		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Mfsd2a	NCBI	NCBI:84879

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