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Protein SLC3A2 PDB 2dh2.png
Available structures
PDB Ortholog search: PDBe RCSB
Aliases SLC3A2, 4F2, 4F2HC, 4T2HC, CD98, CD98HC, MDU1, NACAE, solute carrier family 3 member 2
External IDs MGI: 96955 HomoloGene: 1795 GeneCards: SLC3A2
Gene location (Human)
Human chromosome 11
Chr. Chromosome 11 (human)[1]
Human chromosome 11
Genomic location for SLC3A2
Genomic location for SLC3A2
Band No data available Start 62,856,102 bp[1]
End 62,888,875 bp[1]
RNA expression pattern
PBB GE SLC3A2 200924 s at fs.png
More reference expression data
Species Human Mouse
RefSeq (mRNA)


RefSeq (protein)



Location (UCSC) Chr 11: 62.86 – 62.89 Mb Chr 19: 8.71 – 8.72 Mb
PubMed search [3] [4]
View/Edit Human View/Edit Mouse

4F2 cell-surface antigen heavy chain is a protein that in humans is encoded by the SLC3A2 (solute carrier family 3 member 2) gene.[5][6]

SLC3A2 comprises the heavy subunit of the large neutral amino acid transporter (LAT1) that is also known as CD98 (cluster of differentiation 98).[7][8]


SLC3A2 is a member of the solute carrier family and encodes a cell surface, transmembrane protein with an alpha-amylase domain. The protein exists as the heavy chain of a heterodimer, covalently bound through di-sulfide bonds to one of several possible light chains. It associates with integrins and mediates integrin-dependent signaling related to normal cell growth and tumorigenesis. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.[6]

LAT1 is a heterodimeric membrane transport protein that preferentially transports neutral branched (valine, leucine, isoleucine) and aromatic (tryptophan, tyrosine) amino acids.[9] LAT is highly expressed in brain capillaries (which form the blood brain barrier) relative to other tissues.[9]

A functional LAT1 transporter is composed of two proteins encoded by two distinct genes:

  • 4F2hc/CD98 heavy subunit protein encoded by the SLC3A2 gene (this gene)[10]
  • CD98 light subunit protein encoded by the SLC7A5 gene[11]


SLC3A2 has been shown to interact with SLC7A7.[12]

See also[edit]


  1. ^ a b c GRCh38: Ensembl release 89: ENSG00000168003 - Ensembl, May 2017
  2. ^ a b c GRCm38: Ensembl release 89: ENSMUSG00000010095 - Ensembl, May 2017
  3. ^ "Human PubMed Reference:". 
  4. ^ "Mouse PubMed Reference:". 
  5. ^ Teixeira S, Di Grandi S, Kühn LC (Aug 1987). "Primary structure of the human 4F2 antigen heavy chain predicts a transmembrane protein with a cytoplasmic NH2 terminus". J Biol Chem. 262 (20): 9574–80. PMID 3036867. 
  6. ^ a b "Entrez Gene: SLC3A2 solute carrier family 3 (activators of dibasic and neutral amino acid transport), member 2". 
  7. ^ Kucharzik T, Lugering A, Yan Y, Driss A, Charrier L, Sitaraman S, Merlin D (2005). "Activation of epithelial CD98 glycoprotein perpetuates colonic inflammation". Lab. Invest. 85 (7): 932–41. PMID 15880135. doi:10.1038/labinvest.3700289. 
  8. ^ Lemaître G, Gonnet F, Vaigot P, Gidrol X, Martin MT, Tortajada J, Waksman G (2005). "CD98, a novel marker of transient amplifying human keratinocytes". Proteomics. 5 (14): 3637–45. PMID 16097038. doi:10.1002/pmic.200401224. 
  9. ^ a b Boado RJ, Li JY, Nagaya M, Zhang C, Pardridge WM (1999). "Selective expression of the large neutral amino acid transporter at the blood–brain barrier". Proc. Natl. Acad. Sci. U.S.A. 96 (21): 12079–84. PMC 18415Freely accessible. PMID 10518579. doi:10.1073/pnas.96.21.12079. 
  10. ^ Palacín M, Kanai Y (2004). "The ancillary proteins of HATs: SLC3 family of amino acid transporters". Pflugers Arch. 447 (5): 490–494. PMID 14770309. doi:10.1007/s00424-003-1062-7. 
  11. ^ Verrey F, Closs EI, Wagner CA, Palacin M, Endou H, Kanai Y (2004). "CATs and HATs: the SLC7 family of amino acid transporters". Pflugers Arch. 447 (5): 532–542. PMID 14770310. doi:10.1007/s00424-003-1086-z. 
  12. ^ Pfeiffer R, Rossier G, Spindler B, Meier C, Kühn L, Verrey F (Jan 1999). "Amino acid transport of y+L-type by heterodimers of 4F2hc/CD98 and members of the glycoprotein-associated amino acid transporter family". EMBO J. 18 (1): 49–57. PMC 1171101Freely accessible. PMID 9878049. doi:10.1093/emboj/18.1.49. 

Further reading[edit]

External links[edit]

This article incorporates text from the United States National Library of Medicine, which is in the public domain.