Seroatlas · Human Serome Atlas

IL7

Interleukin-7

Also known as: IL-7, IL7_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
P13232
Gene
IL7
Ensembl
ENSG00000104432
Chromosome
8
Canonical length
177 aa
Protein class
Cancer-related genes, Disease related genes, Human disease related genes, Plasma proteins, Predicted secreted proteins
Secretome location
Secreted to blood

OverviewNCBI Gene

The protein encoded by this gene is a cytokine important for B and T cell development. This cytokine and the hepatocyte growth factor (HGF) form a heterodimer that functions as a pre-pro-B cell growth-stimulating factor. IL7 is found to be a cofactor for V(D)J rearrangement of the T cell receptor beta (TCRB) during early T cell development. This cytokine can be produced locally by intestinal epithelial and epithelial goblet cells, and may serve as a regulatory factor for intestinal mucosal lymphocytes. IL7 plays an essential role in lymphoid cell survival, and in the maintenance of naive and memory T cells. Alternative splicing results in multiple transcript variants encoding distinct isoforms. Additional splice variants have been described but their presence in normal tissues has not been confirmed. Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can be a potent inducer of proinflammatory cytokines and chemokines which may defend against the infection, but may also mediate destructive lung injury. Elevated serum IL7 levels, together with several other circulating cytokines and chemokines, has been found to be associated with the severity of Coronavirus Disease 19 (COVID-19). [provided by RefSeq, Jul 2020]

Canonical amino-acid sequenceUniProt

177 residues, UniProt reviewed canonical sequence.

>P13232|IL7
     1  MFHVSFRYIF GLPPLILVLL PVASSDCDIE GKDGKQYESV LMVSIDQLLD SMKEIGSNCL
    61  NNEFNFFKRH ICDANKEGMF LFRAARKLRQ FLKMNSTGDF DLHLLKVSEG TTILLNCTGQ
   121  VKGRKPAALG EAQPTKSLEE NKSLKEQKKL NDLCFLKRLL QEIKTCWNKI LMGTKEH

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against IL7 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
Secreted
Secreted
Yes
Transmembrane segments
0
Mean surface accessibility (rSASA)
0.41
Highest tissue expression
8.3 nTPM

Expression across tissuesHPA

Tissue

  • skin: 8.3 nTPM
  • small intestine: 8.2 nTPM
  • lymph node: 8.1 nTPM
  • duodenum: 6.3 nTPM
  • colon: 4.8 nTPM
  • fallopian tube: 4.5 nTPM

Single-cell type

  • epicardial cells: 259 nCPM
  • late spermatids: 247 nCPM
  • lymphatic endothelial cells: 203 nCPM
  • fibro-adipogenic progenitors: 191 nCPM
  • retinal ganglion cells: 178 nCPM
  • cardiomyocytes: 158 nCPM

Immune cell

  • memory B-cell: 9.8 nTPM
  • naive B-cell: 8.8 nTPM
  • T-reg: 7.3 nTPM
  • basophil: 5.2 nTPM
  • myeloid DC: 2.2 nTPM
  • memory CD4 T-cell: 1 nTPM

Brain region

  • hypothalamus: 3.1 nTPM
  • medulla oblongata: 1.9 nTPM
  • thalamus: 1.9 nTPM
  • midbrain: 1.4 nTPM
  • spinal cord: 1.4 nTPM
  • cerebellum: 1.3 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about IL7.

Disease | AllUniProt

Conditions IL7 is implicated in, by any mechanism.

Disease | GeneticClinVar

3 pathogenic / likely-pathogenic of 37 ClinVar records.

Conditions with pathogenic or likely-pathogenic variants.

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)
0.36
gnomAD pLI
0.93
gnomAD missense Z
0.7
DepMap mean gene effect
0.08
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 6% 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 IL7 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 IL7 as an antibody target. Whether an autoantibody or antibody against IL7 could matter depends on whether native IL7 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

IL7 is annotated as secreted, so native IL7 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.

Annotation status

The present source text does not explicitly label IL7 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/IL7. 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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