Seroatlas · Human Serome Atlas

SLC3A2

Amino acid transporter heavy chain SLC3A2

Also known as: 4F2, 4F2_HUMAN, 4F2HC, 4T2HC, CD98, CD98HC, MDU1, NACAE

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
P08195
Gene
SLC3A2
Ensembl
ENSG00000168003
Chromosome
11
Canonical length
630 aa
Protein class
Cancer-related genes, CD markers, Metabolic proteins, Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins, Transporters
Subcellular location
Nucleoplasm,Plasma membrane

OverviewNCBI Gene

This gene is a member of the solute carrier family and encodes a cell surface, transmembrane protein. The protein exists as the heavy chain of a heterodimer, covalently bound through di-sulfide bonds to one of several possible light chains. The encoded transporter plays a role in regulation of intracellular calcium levels and transports L-type amino acids. Alternatively spliced transcript variants, encoding different isoforms, have been characterized. [provided by RefSeq, Nov 2010]

Canonical amino-acid sequenceUniProt

630 residues, UniProt reviewed canonical sequence.

>P08195|SLC3A2
     1  MELQPPEASI AVVSIPRQLP GSHSEAGVQG LSAGDDSELG SHCVAQTGLE LLASGDPLPS
    61  ASQNAEMIET GSDCVTQAGL QLLASSDPPA LASKNAEVTG TMSQDTEVDM KEVELNELEP
   121  EKQPMNAASG AAMSLAGAEK NGLVKIKVAE DEAEAAAAAK FTGLSKEELL KVAGSPGWVR
   181  TRWALLLLFW LGWLGMLAGA VVIIVRAPRC RELPAQKWWH TGALYRIGDL QAFQGHGAGN
   241  LAGLKGRLDY LSSLKVKGLV LGPIHKNQKD DVAQTDLLQI DPNFGSKEDF DSLLQSAKKK
   301  SIRVILDLTP NYRGENSWFS TQVDTVATKV KDALEFWLQA GVDGFQVRDI ENLKDASSFL
   361  AEWQNITKGF SEDRLLIAGT NSSDLQQILS LLESNKDLLL TSSYLSDSGS TGEHTKSLVT
   421  QYLNATGNRW CSWSLSQARL LTSFLPAQLL RLYQLMLFTL PGTPVFSYGD EIGLDAAALP
   481  GQPMEAPVML WDESSFPDIP GAVSANMTVK GQSEDPGSLL SLFRRLSDQR SKERSLLHGD
   541  FHAFSAGPGL FSYIRHWDQN ERFLVVLNFG DVGLSAGLQA SDLPASASLP AKADLLLSTQ
   601  PGREEGSPLE LERLKLEPHE GLLLRFPYAA

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against SLC3A2 can act on the native protein depends on physical access: surface and secreted proteins are reachable by circulating antibodies, intracellular proteins usually are not.

Antibody reachability
Cell surface
Secreted
No
Transmembrane segments
1
Mean surface accessibility (rSASA)
0.41
Highest tissue expression
178 nTPM

Expression across tissuesHPA

Tissue

  • parathyroid gland: 178 nTPM
  • kidney: 147 nTPM
  • basal ganglia: 122 nTPM
  • bone marrow: 115 nTPM
  • skeletal muscle: 112 nTPM
  • skin: 108 nTPM

Single-cell type

  • syncytiotrophoblasts: 1,124 nCPM
  • retinal pigment epithelial cells: 443 nCPM
  • breast lactating cells: 401 nCPM
  • migrating cytotrophoblasts: 289 nCPM
  • basal keratinocytes: 284 nCPM
  • esophageal basal cells: 273 nCPM

Immune cell

  • plasmacytoid DC: 305 nTPM
  • total PBMC: 186 nTPM
  • MAIT T-cell: 158 nTPM
  • classical monocyte: 149 nTPM
  • intermediate monocyte: 148 nTPM
  • non-classical monocyte: 124 nTPM

Brain region

  • thalamus: 139 nTPM
  • cerebellum: 105 nTPM
  • medulla oblongata: 103 nTPM
  • basal ganglia: 99 nTPM
  • spinal cord: 98 nTPM
  • pons: 93 nTPM

ReferencesPubMed · IEDB

Publications for SLC3A2 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.

Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.

Genetic constraint and essentialitygnomAD · DepMap

Does the body need this protein intact? Low LOEUF or a strong DepMap dependency means loss or blockade of the protein is likely to be felt.

gnomAD LOEUF (loss-of-function intolerance)
0.91
gnomAD pLI
0
gnomAD missense Z
1.15
DepMap mean gene effect
-0.5
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of SLC3A2 in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads SLC3A2 as an antibody target. Whether an autoantibody or antibody against SLC3A2 could matter depends on whether native SLC3A2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

SLC3A2 is annotated at the cell surface, where native SLC3A2 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.

Annotation status

The present source text does not explicitly label SLC3A2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/SLC3A2. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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