Seroatlas · Human Serome Atlas

CD7

T-cell antigen CD7

Also known as: CD7_HUMAN, GP40, LEU-9, Tp40, TP41

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

Protein identityUniProt · HPA

UniProt accession
P09564
Gene
CD7
Ensembl
ENSG00000173762
Chromosome
17
Canonical length
240 aa
Protein class
CD markers, Predicted intracellular proteins, Predicted membrane proteins

OverviewNCBI Gene

This gene encodes a transmembrane protein which is a member of the immunoglobulin superfamily. This protein is found on thymocytes and mature T cells. It plays an essential role in T-cell interactions and also in T-cell/B-cell interaction during early lymphoid development. [provided by RefSeq, Jul 2008]

Canonical amino-acid sequenceUniProt

240 residues, UniProt reviewed canonical sequence.

>P09564|CD7
     1  MAGPPRLLLL PLLLALARGL PGALAAQEVQ QSPHCTTVPV GASVNITCST SGGLRGIYLR
    61  QLGPQPQDII YYEDGVVPTT DRRFRGRIDF SGSQDNLTIT MHRLQLSDTG TYTCQAITEV
   121  NVYGSGTLVL VTEEQSQGWH RCSDAPPRAS ALPAPPTGSA LPDPQTASAL PDPPAASALP
   181  AALAVISFLL GLGLGVACVL ARTQIKKLCS WRDKNSAACV VYEDMSHSRC NTLSSPNQYQ

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CD7 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)
0.48
Highest tissue expression
51 nTPM

Expression across tissuesHPA

Tissue

  • spleen: 51 nTPM
  • thymus: 45 nTPM
  • lymph node: 35 nTPM
  • appendix: 31 nTPM
  • bone marrow: 27 nTPM
  • small intestine: 20 nTPM

Single-cell type

  • nk-cells: 774 nCPM
  • thymocytes: 373 nCPM
  • innate lymphoid cells: 333 nCPM
  • t-cells: 307 nCPM
  • pdcs: 26 nCPM
  • mast cells: 20 nCPM

Immune cell

  • NK-cell: 232 nTPM
  • naive CD8 T-cell: 72 nTPM
  • naive CD4 T-cell: 70 nTPM
  • gdT-cell: 67 nTPM
  • MAIT T-cell: 58 nTPM
  • memory CD8 T-cell: 49 nTPM

Brain region

  • medulla oblongata: 2.4 nTPM
  • cerebral cortex: 2.2 nTPM
  • spinal cord: 2 nTPM
  • white matter: 2 nTPM
  • hypothalamus: 1.7 nTPM
  • pons: 1.7 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)
1.07
gnomAD pLI
0.05
gnomAD missense Z
0.54
DepMap mean gene effect
-0.11
DepMap dependency class
selective

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% 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 CD7 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 CD7 as an antibody target. Whether an autoantibody or antibody against CD7 could matter depends on whether native CD7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CD7 is annotated at the cell surface, where native CD7 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 CD7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CD7. 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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