ENOX2
Ecto-NOX disulfide-thiol exchanger 2
Also known as: APK1, COVA1, ENOX2_HUMAN, tNOX
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q16206
- Gene
- ENOX2
- Ensembl
- ENSG00000165675
- Chromosome
- X
- Canonical length
- 610 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Plasma membrane,Cytosol
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
This gene is a tumor-specific member of the ECTO-NOX family of genes that encode cell surface NADH oxidases. The encoded protein has two enzymatic activities: catalysis of hydroquinone or NADH oxidation, and protein disulfide interchange. The protein also displays prion-like properties. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Aug 2013]
Canonical amino-acid sequenceUniProt
610 residues, UniProt reviewed canonical sequence.
>Q16206|ENOX2
1 MQRDFRWLWV YEIGYAADNS RTLNVDSTAM TLPMSDPTAW ATAMNNLGMA PLGIAGQPIL
61 PDFDPALGMM TGIPPITPMM PGLGIVPPPI PPDMPVVKEI IHCKSCTLFP PNPNLPPPAT
121 RERPPGCKTV FVGGLPENGT EQIIVEVFEQ CGEIIAIRKS KKNFCHIRFA EEYMVDKALY
181 LSGYRIRLGS STDKKDTGRL HVDFAQARDD LYEWECKQRM LAREERHRRR MEEERLRPPS
241 PPPVVHYSDH ECSIVAEKLK DDSKFSEAVQ TLLTWIERGE VNRRSANNFY SMIQSANSHV
301 RRLVNEKAAH EKDMEEAKEK FKQALSGILI QFEQIVAVYH SASKQKAWDH FTKAQRKNIS
361 VWCKQAEEIR NIHNDELMGI RREEEMEMSD DEIEEMTETK ETEESALVSQ AEALKEENDS
421 LRWQLDAYRN EVELLKQEQG KVHREDDPNK EQQLKLLQQA LQGMQQHLLK VQEEYKKKEA
481 ELEKLKDDKL QVEKMLENLK EKESCASRLC ASNQDSEYPL EKTMNSSPIK SEREALLVGI
541 ISTFLHVHPF GASIEYICSY LHRLDNKICT SDVECLMGRL QHTFKQEMTG VGASLEKRWK
601 FCGFEGLKLTLocalizationUniProt · AlphaFold · HPA
Whether an antibody against ENOX2 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
- Mean surface accessibility (rSASA)
- 0.46
- Highest tissue expression
- 9.3 nTPM
Expression across tissuesHPA
Tissue
- heart muscle: 9.3 nTPM
- tonsil: 8 nTPM
- endometrium: 7.8 nTPM
- thymus: 7.5 nTPM
- tongue: 7.4 nTPM
- lymph node: 7.3 nTPM
Single-cell type
- sertoli cells: 189 nCPM
- oligodendrocytes: 171 nCPM
- salivary ionocytes: 151 nCPM
- myonuclei: 149 nCPM
- adrenal medulla cells: 149 nCPM
- kupffer cells: 123 nCPM
Immune cell
- intermediate monocyte: 14 nTPM
- eosinophil: 13 nTPM
- T-reg: 12 nTPM
- naive B-cell: 12 nTPM
- memory B-cell: 11 nTPM
- naive CD4 T-cell: 11 nTPM
Brain region
- basal ganglia: 17 nTPM
- white matter: 17 nTPM
- hypothalamus: 15 nTPM
- thalamus: 14 nTPM
- medulla oblongata: 14 nTPM
- cerebral cortex: 13 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)
- 0.89
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.83
- DepMap mean gene effect
- 0.1
- 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
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads ENOX2 as an antibody target. Whether an autoantibody or antibody against ENOX2 could matter depends on whether native ENOX2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
ENOX2 is annotated at the cell surface, where native ENOX2 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 ENOX2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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