NPTXR
Neuronal pentraxin receptor
Also known as: NPTXR_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- O95502
- Gene
- NPTXR
- Ensembl
- ENSG00000221890
- Chromosome
- 22
- Canonical length
- 500 aa
- Protein class
- Plasma proteins, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Plasma membrane,Cytosol
- Secretome location
- Intracellular and membrane
OverviewNCBI Gene
This gene encodes a protein similar to the rat neuronal pentraxin receptor. The rat pentraxin receptor is an integral membrane protein that is thought to mediate neuronal uptake of the snake venom toxin, taipoxin, and its transport into the synapses. Studies in rat indicate that translation of this mRNA initiates at a non-AUG (CUG) codon. This may also be true for mouse and human, based on strong sequence conservation amongst these species. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
500 residues, UniProt reviewed canonical sequence.
>O95502|NPTXR
1 MKFLAVLLAA GMLAFLGAVI CIIASVPLAA SPARALPGGA DNASVASGAA ASPGPQRSLS
61 ALHGAGGSAG PPALPGAPAA SAHPLPPGPL FSRFLCTPLA AACPSGAQQG DAAGAAPGER
121 EELLLLQSTA EQLRQTALQQ EARIRADQDT IRELTGKLGR CESGLPRGLQ GAGPRRDTMA
181 DGPWDSPALI LELEDAVRAL RDRIDRLEQE LPARVNLSAA PAPVSAVPTG LHSKMDQLEG
241 QLLAQVLALE KERVALSHSS RRQRQEVEKE LDVLQGRVAE LEHGSSAYSP PDAFKISIPI
301 RNNYMYARVR KALPELYAFT ACMWLRSRSS GTGQGTPFSY SVPGQANEIV LLEAGHEPME
361 LLINDKVAQL PLSLKDNGWH HICIAWTTRD GLWSAYQDGE LQGSGENLAA WHPIKPHGIL
421 ILGQEQDTLG GRFDATQAFV GDIAQFNLWD HALTPAQVLG IANCTAPLLG NVLPWEDKLV
481 EAFGGATKAA FDVCKGRAKALocalizationUniProt · AlphaFold · HPA
Whether an antibody against NPTXR 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
- Unknown
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.46
- Highest tissue expression
- 179 nTPM
Expression across tissuesHPA
Tissue
- hippocampal formation: 179 nTPM
- cerebral cortex: 131 nTPM
- amygdala: 111 nTPM
- cerebellum: 47 nTPM
- hypothalamus: 42 nTPM
- blood vessel: 21 nTPM
Single-cell type
- brain excitatory neurons: 101 nCPM
- brain inhibitory neurons: 51 nCPM
- other brain neurons: 40 nCPM
- oligodendrocyte progenitor cells: 30 nCPM
- retinal amacrine cells: 26 nCPM
- endometrial secretory cells: 21 nCPM
Immune cell
- memory CD8 T-cell: 0.3 nTPM
- gdT-cell: 0.2 nTPM
- MAIT T-cell: 0.2 nTPM
- naive CD4 T-cell: 0.2 nTPM
- naive CD8 T-cell: 0.2 nTPM
- basophil: 0.1 nTPM
Brain region
- hippocampal formation: 654 nTPM
- cerebral cortex: 366 nTPM
- amygdala: 254 nTPM
- basal ganglia: 218 nTPM
- thalamus: 186 nTPM
- white matter: 160 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)
- 0.49
- gnomAD pLI
- 0.72
- gnomAD missense Z
- 1.26
- DepMap mean gene effect
- 0
- DepMap dependency class
- selective
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 5% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NPTXR in the human serome: UniProt-annotated complex subunits plus reported interactors. Each links to its own Seroatlas record.
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads NPTXR as an antibody target. Whether an autoantibody or antibody against NPTXR could matter depends on whether native NPTXR is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NPTXR 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 NPTXR as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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