TSPAN32
Tetraspanin-32
Also known as: PHEMX, TSN32_HUMAN, TSSC6
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q96QS1
- Gene
- TSPAN32
- Ensembl
- ENSG00000064201
- Chromosome
- 11
- Canonical length
- 320 aa
- Protein class
- Predicted membrane proteins
- Subcellular location
- Nucleoplasm
OverviewNCBI Gene
This gene, which is a member of the tetraspanin superfamily, is one of several tumor-suppressing subtransferable fragments located in the imprinted gene domain of chromosome 11p15.5, an important tumor-suppressor gene region. Alterations in this region have been associated with Beckwith-Wiedemann syndrome, Wilms tumor, rhabdomyosarcoma, adrenocortical carcinoma, and lung, ovarian and breast cancers. This gene is located among several imprinted genes; however, this gene, as well as the tumor-suppressing subchromosomal transferable fragment 4, escapes imprinting. This gene may play a role in malignancies and diseases that involve this region, and it is also involved in hematopoietic cell function. Alternatively spliced transcript variants have been described, but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
320 residues, UniProt reviewed canonical sequence.
>Q96QS1|TSPAN32
1 MGPWSRVRVA KCQMLVTCFF ILLLGLSVAT MVTLTYFGAH FAVIRRASLE KNPYQAVHQW
61 AFSAGLSLVG LLTLGAVLSA AATVREAQGL MAGGFLCFSL AFCAQVQVVF WRLHSPTQVE
121 DAMLDTYDLV YEQAMKGTSH VRRQELAAIQ DVFLCCGKKS PFSRLGSTEA DLCQGEEAAR
181 EDCLQGIRSF LRTHQQVASS LTSIGLALTV SALLFSSFLW FAIRCGCSLD RKGKYTLTPR
241 ACGRQPQEPS LLRCSQGGPT HCLHSEAVAI GPRGCSGSLR WLQESDAAPL PLSCHLAAHR
301 ALQGRSRGGL SGCPERGLSDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against TSPAN32 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
- 4
- Mean surface accessibility (rSASA)
- 0.42
- Highest tissue expression
- 19 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 19 nTPM
- heart muscle: 11 nTPM
- lymph node: 5.2 nTPM
- spleen: 3.3 nTPM
- tonsil: 2.3 nTPM
- lung: 1.9 nTPM
Single-cell type
- platelets: 116 nCPM
- megakaryocyte progenitors: 85 nCPM
- megakaryocyte-erythroid progenitors: 59 nCPM
- hematopoietic stem cells: 59 nCPM
- nk-cells: 55 nCPM
- megakaryocytes: 43 nCPM
Immune cell
- NK-cell: 59 nTPM
- non-classical monocyte: 46 nTPM
- intermediate monocyte: 41 nTPM
- basophil: 41 nTPM
- myeloid DC: 32 nTPM
- classical monocyte: 32 nTPM
Brain region
- cerebellum: 3 nTPM
- medulla oblongata: 2.9 nTPM
- white matter: 2.9 nTPM
- midbrain: 2.6 nTPM
- pons: 2.6 nTPM
- cerebral cortex: 2.5 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)
- 0.99
- gnomAD pLI
- 0
- gnomAD missense Z
- -0.33
- DepMap mean gene effect
- 0.01
- DepMap dependency class
- none
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
- cell-cell signaling
- cytoskeleton organization
- defense response to protozoan
- integrin-mediated signaling pathway
- negative regulation of myeloid dendritic cell activation
- negative regulation of T cell proliferation
- platelet aggregation
- regulation of defense response to virus
- regulation of vascular endothelial growth factor signaling pathway
- T cell proliferation
Cellular components
Protein domainsUniProt · Pfam · InterPro
- Tetraspanin, EC2 domain superfamily
- Tetraspanin/Peripherin
- Tetraspanin family
- Tetraspanin-32, extracellular domain
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads TSPAN32 as an antibody target. Whether an autoantibody or antibody against TSPAN32 could matter depends on whether native TSPAN32 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
TSPAN32 is annotated at the cell surface, where native TSPAN32 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 TSPAN32 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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