VSIR
V-type immunoglobulin domain-containing suppressor of T-cell activation
Also known as: B7-H5, B7H5, C10orf54, Dies1, GI24, PD-1H, SISP1, VISTA, VISTA_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q9H7M9
- Gene
- VSIR
- Ensembl
- ENSG00000107738
- Chromosome
- 10
- Canonical length
- 311 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
Enables endopeptidase activator activity; enzyme binding activity; and identical protein binding activity. Involved in several processes, including negative regulation of cytokine production; positive regulation of metabolic process; and regulation of T cell activation. Located in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
311 residues, UniProt reviewed canonical sequence.
>Q9H7M9|VSIR
1 MGVPTALEAG SWRWGSLLFA LFLAASLGPV AAFKVATPYS LYVCPEGQNV TLTCRLLGPV
61 DKGHDVTFYK TWYRSSRGEV QTCSERRPIR NLTFQDLHLH HGGHQAANTS HDLAQRHGLE
121 SASDHHGNFS ITMRNLTLLD SGLYCCLVVE IRHHHSEHRV HGAMELQVQT GKDAPSNCVV
181 YPSSSQDSEN ITAAALATGA CIVGILCLPL ILLLVYKQRQ AASNRRAQEL VRMDSNIQGI
241 ENPGFEASPP AQGIPEAKVR HPLSYVAQRQ PSESGRHLLS EPSTPLSPPG PGDVFFPSLD
301 PVPDSPNFEV ILocalizationUniProt · AlphaFold · HPA
Whether an antibody against VSIR 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)
- 0.46
- Highest tissue expression
- 88 nTPM
Expression across tissuesHPA
Tissue
- spleen: 88 nTPM
- bone marrow: 77 nTPM
- adipose tissue: 39 nTPM
- lung: 34 nTPM
- appendix: 30 nTPM
- breast: 28 nTPM
Single-cell type
- neutrophils: 1,249 nCPM
- syncytiotrophoblasts: 844 nCPM
- extravillous trophoblasts: 424 nCPM
- cytotrophoblasts: 409 nCPM
- monocytes: 387 nCPM
- esophageal apical cells: 350 nCPM
Immune cell
- neutrophil: 1,008 nTPM
- eosinophil: 769 nTPM
- total PBMC: 471 nTPM
- non-classical monocyte: 437 nTPM
- classical monocyte: 401 nTPM
- intermediate monocyte: 372 nTPM
Brain region
- medulla oblongata: 43 nTPM
- thalamus: 38 nTPM
- midbrain: 33 nTPM
- hypothalamus: 31 nTPM
- basal ganglia: 30 nTPM
- spinal cord: 30 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)
- 0.47
- gnomAD pLI
- 0.76
- DepMap mean gene effect
- 0.06
- DepMap dependency class
- none
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
- negative regulation of alpha-beta T cell activation
- negative regulation of CD4-positive, alpha-beta T cell proliferation
- negative regulation of CD8-positive, alpha-beta T cell proliferation
- negative regulation of interleukin-10 production
- negative regulation of interleukin-17 production
- negative regulation of tumor necrosis factor production
- negative regulation of type II interferon production
- positive regulation of cell migration
- positive regulation of endopeptidase activity
- positive regulation of gene expression
- positive regulation of regulatory T cell differentiation
- regulation of immune response
- zymogen activation
- positive regulation of collagen catabolic process
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Immunoglobulin domain subtype
- Immunoglobulin-like domain
- Immunoglobulin V-set domain
- Immunoglobulin-like fold
- Immunoglobulin-like domain superfamily
- Immunoglobulin V-set domain
- V-type immunoglobulin domain-containing suppressor of T-cell activation
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads VSIR as an antibody target. Whether an autoantibody or antibody against VSIR could matter depends on whether native VSIR is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
VSIR is annotated at the cell surface, where native VSIR 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 VSIR as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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