Seroatlas · Human Serome Atlas

IGHG4

Immunoglobulin heavy constant gamma 4

Also known as: IGHG4_HUMAN

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

Protein identityUniProt · HPA

UniProt accession
P01861
Gene
IGHG4
Ensembl
ENSG00000211892
Chromosome
14
Canonical length
396 aa
Protein class
FDA approved drug targets, Immunoglobulin genes, Plasma proteins, Predicted intracellular proteins, Predicted membrane proteins, Predicted secreted proteins
Secretome location
Immunoglobulin genes

OverviewNCBI Gene

Predicted to enable antigen binding activity and immunoglobulin receptor binding activity. Predicted to be involved in antibacterial humoral response and complement activation, classical pathway. Located in blood microparticle and extracellular exosome. [provided by Alliance of Genome Resources, Jul 2025]

Canonical amino-acid sequenceUniProt

396 residues, UniProt reviewed canonical sequence.

>P01861|IGHG4
     1  ASTKGPSVFP LAPCSRSTSE STAALGCLVK DYFPEPVTVS WNSGALTSGV HTFPAVLQSS
    61  GLYSLSSVVT VPSSSLGTKT YTCNVDHKPS NTKVDKRVES KYGPPCPSCP APEFLGGPSV
   121  FLFPPKPKDT LMISRTPEVT CVVVDVSQED PEVQFNWYVD GVEVHNAKTK PREEQFNSTY
   181  RVVSVLTVLH QDWLNGKEYK CKVSNKGLPS SIEKTISKAK GQPREPQVYT LPPSQEEMTK
   241  NQVSLTCLVK GFYPSDIAVE WESNGQPENN YKTTPPVLDS DGSFFLYSRL TVDKSRWQEG
   301  NVFSCSVMHE ALHNHYTQKS LSLSLELQLE ESCAEAQDGE LDGLWTTITI FITLFLLSVC
   361  YSATVTFFKV KWIFSSVVDL KQTIVPDYRN MIRQGA

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against IGHG4 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
0
Highest tissue expression
2,338 nTPM

Expression across tissuesHPA

Tissue

  • appendix: 2,338 nTPM
  • spleen: 825 nTPM
  • tonsil: 819 nTPM
  • urinary bladder: 554 nTPM
  • esophagus: 376 nTPM
  • thyroid gland: 320 nTPM

Single-cell type

  • plasma cells: 120 nCPM
  • lymphatic endothelial cells: 16 nCPM
  • b-cells: 1.9 nCPM
  • mesothelial cells: 1.3 nCPM
  • mucous neck cells: 0.8 nCPM
  • foveolar cells: 0.6 nCPM

Immune cell

  • memory B-cell: 123 nTPM
  • naive B-cell: 74 nTPM
  • total PBMC: 20 nTPM
  • neutrophil: 0.2 nTPM
  • eosinophil: 0.1 nTPM
  • myeloid DC: 0.1 nTPM

Brain region

  • pons: 2.3 nTPM
  • spinal cord: 1.9 nTPM
  • cerebral cortex: 1 nTPM
  • medulla oblongata: 0.9 nTPM
  • basal ganglia: 0.8 nTPM
  • cerebellum: 0.5 nTPM

DiseaseUniProt · ClinVar · IEDB · PubMed

Four sources answering four different questions about IGHG4.

Disease | ImmuneIEDB

Conditions an epitope on IGHG4 was assayed in.

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads IGHG4 as an antibody target. Whether an autoantibody or antibody against IGHG4 could matter depends on whether native IGHG4 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

IGHG4 is annotated at the cell surface, where native IGHG4 is exposed to circulating antibodies and is a prime autoantibody target that could block, deplete, or overstimulate it.

Source-annotated serology context

The source annotations explicitly mention antibody, autoantibody, autoantigen, or autoimmune context. This is biological context, not study-specific reactivity.

  • Predicted to be involved in antibacterial humoral response and complement activation, classical pathway.

Canonical record: https://seroatlas.com/gene/IGHG4. 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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