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 SIVLocalizationUniProt · 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
- adaptive immune response
- cell recognition
- detection of stimulus
- detection of tumor cell
- establishment of T cell polarity
- heterophilic cell-cell adhesion via plasma membrane cell adhesion molecules
- lymphocyte migration into lymphoid organs
- negative regulation of activated T cell proliferation
- positive regulation of cytokine production
- positive regulation of natural killer cell mediated cytotoxicity
- positive regulation of natural killer cell mediated cytotoxicity directed against tumor cell target
- positive regulation of type II interferon production
- regulation of T cell activation
- regulation of T cell differentiation
- regulation of CD8-positive, alpha-beta T cell activation
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.
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