Seroatlas · Human Serome Atlas

CRTAM

Cytotoxic and regulatory T-cell molecule

Also known as: CD355, CRTAM_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
O95727
Gene
CRTAM
Ensembl
ENSG00000109943
Chromosome
11
Canonical length
393 aa
Protein class
CD markers, Predicted membrane proteins
Quaternary structure
Homodimer

OverviewNCBI Gene

The CRTAM gene is upregulated in CD4 (see MIM 186940)-positive and CD8 (see CD8A; MIM 186910)-positive T cells and encodes a type I transmembrane protein with V and C1-like Ig domains (Yeh et al., 2008 [PubMed 18329370]).[supplied by OMIM, Feb 2009]

Canonical amino-acid sequenceUniProt

393 residues, UniProt reviewed canonical sequence.

>O95727|CRTAM
     1  MWWRVLSLLA WFPLQEASLT NHTETITVEE GQTLTLKCVT SLRKNSSLQW LTPSGFTIFL
    61  NEYPALKNSK YQLLHHSANQ LSITVPNVTL QDEGVYKCLH YSDSVSTKEV KVIVLATPFK
   121  PILEASVIRK QNGEEHVVLM CSTMRSKPPP QITWLLGNSM EVSGGTLHEF ETDGKKCNTT
   181  STLIIHTYGK NSTVDCIIRH RGLQGRKLVA PFRFEDLVTD EETASDALER NSLSSQDPQQ
   241  PTSTVSVTED SSTSEIDKEE KEQTTQDPDL TTEANPQYLG LARKKSGILL LTLVSFLIFI
   301  LFIIVQLFIM KLRKAHVIWK KENEVSEHTL ESYRSRSNNE ETSSEEKNGQ SSHPMRCMNY
   361  ITKLYSEAKT KRKENVQHSK LEEKHIQVPE SIV

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CRTAM 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)
0.45
Highest tissue expression
128 nTPM

Expression across tissuesHPA

Tissue

  • cerebellum: 128 nTPM
  • lymph node: 8.2 nTPM
  • thymus: 4.5 nTPM
  • spleen: 3.3 nTPM
  • tonsil: 3.2 nTPM
  • spinal cord: 2.5 nTPM

Single-cell type

  • t-cells: 128 nCPM
  • nk-cells: 74 nCPM
  • brain excitatory neurons: 53 nCPM
  • innate lymphoid cells: 21 nCPM
  • thymocytes: 21 nCPM
  • monocytes: 10 nCPM

Immune cell

  • NK-cell: 54 nTPM
  • naive CD8 T-cell: 33 nTPM
  • memory CD8 T-cell: 27 nTPM
  • gdT-cell: 13 nTPM
  • MAIT T-cell: 13 nTPM
  • non-classical monocyte: 10 nTPM

Brain region

  • cerebellum: 79 nTPM
  • pons: 8.9 nTPM
  • white matter: 3.6 nTPM
  • midbrain: 3.2 nTPM
  • cerebral cortex: 3.1 nTPM
  • medulla oblongata: 2.7 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)
1.17
gnomAD pLI
0
gnomAD missense Z
0.37
DepMap mean gene effect
-0.05
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% 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

Antibody and autoantibody relevanceSeroatlas analysis

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

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

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