SELENOV
Selenoprotein V
Also known as: SELV, SELV_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P59797
- Gene
- SELENOV
- Ensembl
- ENSG00000186838
- Chromosome
- 19
- Canonical length
- 346 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a selenoprotein containing a selenocysteine (Sec) residue, which is encoded by the UGA codon that normally signals translation termination. The 3' UTRs of selenoprotein mRNAs contain a conserved stem-loop structure, the Sec insertion sequence (SECIS) element, which is necessary for the recognition of UGA as a Sec codon rather than as a stop signal. This protein is specifically expressed in the testis. It belongs to the SelWTH family, which possesses a thioredoxin-like fold and a conserved CxxU (C is cysteine, U is Sec) motif, suggesting a redox function for this gene. Alternatively spliced transcript variants have been found for this gene.[provided by RefSeq, Apr 2017]
Canonical amino-acid sequenceUniProt
346 residues, UniProt reviewed canonical sequence.
>P59797|SELENOV
1 MNNQARTPAP SSARTSTSVR ASTPTRTPTP LRTPTPVRTR TPIRTLTPVL TPSPAGTSPL
61 VLTPAPAQIP TLVPTPALAR IPRLVPPPAP AWIPTPVPTP VPVRNPTPVP TPARTLTPPV
121 RVPAPAPAQL LAGIRAALPV LDSYLAPALP LDPPPEPAPE LPLLPEEDPE PAPSLKLIPS
181 VSSEAGPAPG PLPTRTPLAA NSPGPTLDFT FRADPSAIGL ADPPIPSPVP SPILGTIPSA
241 ISLQNCTETF PSSSENFALD KRVLIRVTYC GLUSYSLRYI LLKKSLEQQF PNHLLFEEDR
301 AAQATGEFEV FVNGRLVHSK KRGDGFVNES RLQKIVSVID EEIKKRLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SELENOV 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
- Intracellular
- Secreted
- No
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0
- Highest tissue expression
- 9.4 nTPM
Expression across tissuesHPA
Tissue
- testis: 9.4 nTPM
- parathyroid gland: 2.2 nTPM
- thyroid gland: 1.5 nTPM
- retina: 0.2 nTPM
- amygdala: 0.1 nTPM
- basal ganglia: 0.1 nTPM
Single-cell type
- late spermatids: 423 nCPM
- early spermatids: 102 nCPM
- late primary spermatocytes: 68 nCPM
- epididymal basal cells: 9.9 nCPM
- breast myoepithelial cells: 7.7 nCPM
- retinal amacrine cells: 6.9 nCPM
Immune cell
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
- MAIT T-cell: 0 nTPM
Brain region
- white matter: 3.2 nTPM
- cerebellum: 3.1 nTPM
- medulla oblongata: 3 nTPM
- cerebral cortex: 2.5 nTPM
- pons: 2.5 nTPM
- hypothalamus: 2.4 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)
- 1.92
- gnomAD pLI
- 0
- DepMap mean gene effect
- 0.03
- 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
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads SELENOV as an antibody target. Whether an autoantibody or antibody against SELENOV could matter depends on whether native SELENOV is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SELENOV is annotated as predominantly intracellular. Intracellular proteins are common autoantibody markers, becoming visible to the immune system after cell injury or altered processing, but are usually markers of disease rather than direct drivers.
Annotation status
The present source text does not explicitly label SELENOV as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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