MFSD2 lysolipid transporter A, lysophospholipid

Summary
Gene Symbol
  • MFSD2A
Organism
Homo sapiens (human)
NCBI Gene
84879
PubChem
84879
Alliance of Genome Resources
JoGo
MFSD2A
TogoVar
MFSD2A
Annotation
Keyword
  • 3D-structure
  • Alternative splicing
  • Cell membrane
  • Disease variant
  • Disulfide bond
  • Endoplasmic reticulum
  • Glycoprotein
  • Lipid transport
  • Primary microcephaly
  • Proteomics identification
  • Reference proteome
  • Symport
  • Transmembrane helix
Proteins
Displaying all 4 entries
UniProt Protein Name
Q71RE4
B4DNN7
  • Major facilitator superfamily domain-containing protein 2A
E7EPI8
Q8NA29
  • Major facilitator superfamily domain-containing protein 2A
Gene Ontology (GO)
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying 1 entry
DO ID Disease Name Source
DOID:0070277 primary autosomal recessive microcephaly 15

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: April 6, 2026