Seroatlas · Human Serome Atlas

MS4A10

Membrane-spanning 4-domains subfamily A member 10

Also known as: CD20L7, M4A10_HUMAN, MS4A9

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

Protein identityUniProt · HPA

UniProt accession
Q96PG2
Gene
MS4A10
Ensembl
ENSG00000172689
Chromosome
11
Canonical length
267 aa
Protein class
Predicted membrane proteins, Transporters

OverviewNCBI Gene

Most MS4A genes, including MS4A10, encode proteins with at least 4 potential transmembrane domains and N- and C-terminal cytoplasmic domains encoded by distinct exons.[supplied by OMIM, Apr 2004]

Canonical amino-acid sequenceUniProt

267 residues, UniProt reviewed canonical sequence.

>Q96PG2|MS4A10
     1  MKAEATVIPS RCARGLPSWQ VLSPVQPWQT SAPQNTTQPK LLAPHQHEKS QKKSSLLKEL
    61  GAFHITIALL HLVFGGYLAS IVKNLHLVVL KSWYPFWGAA SFLISGILAI TMKTFSKTYL
   121  KMLCLMTNLI SLFCVLSGLF VISKDLFLES PFESPIWRMY PNSTVHIQRL ELALLCFTVL
   181  ELFLPVPTAV TAWRGDCPSA KNDDACLVPN TPLHLKGLPV EPPPSYQSVI QGDAQHKQHQ
   241  RLREVKQVAP DTWIVTDGAA IWTQTAN

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against MS4A10 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
4
Mean surface accessibility (rSASA)
0.46
Highest tissue expression
81 nTPM

Expression across tissuesHPA

Tissue

  • small intestine: 81 nTPM
  • duodenum: 69 nTPM
  • kidney: 0.7 nTPM
  • bone marrow: 0.3 nTPM
  • colon: 0.3 nTPM
  • skeletal muscle: 0.3 nTPM

Single-cell type

  • enterocytes: 340 nCPM
  • early spermatids: 6.8 nCPM
  • neuroendocrine cells: 4.6 nCPM
  • enteric transient amplifying cells: 4.3 nCPM
  • paneth cells: 3.9 nCPM
  • proximal tubule cells: 2.6 nCPM

Immune cell

  • basophil: 0.7 nTPM
  • neutrophil: 0.2 nTPM
  • naive B-cell: 0.1 nTPM
  • NK-cell: 0.1 nTPM
  • plasmacytoid DC: 0.1 nTPM
  • classical monocyte: 0 nTPM

Brain region

  • cerebellum: 2 nTPM
  • cerebral cortex: 1.7 nTPM
  • choroid plexus: 1.7 nTPM
  • white matter: 1.7 nTPM
  • amygdala: 1.6 nTPM
  • basal ganglia: 1.5 nTPM

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)
1.82
gnomAD pLI
0
gnomAD missense Z
-0.19
DepMap mean gene effect
-0.08
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

InteractionsUniProt · HPA

Protein binding partners of MS4A10 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 MS4A10 as an antibody target. Whether an autoantibody or antibody against MS4A10 could matter depends on whether native MS4A10 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

MS4A10 is annotated at the cell surface, where native MS4A10 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 MS4A10 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/MS4A10. 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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