NSG1
Neuronal vesicle trafficking-associated protein 1
Also known as: D4S234E, NEEP21, NSG1_HUMAN, P21
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P42857
- Gene
- NSG1
- Ensembl
- ENSG00000168824
- Chromosome
- 4
- Canonical length
- 185 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
Predicted to enable clathrin light chain binding activity. Involved in apoptotic process. Located in endoplasmic reticulum. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
185 residues, UniProt reviewed canonical sequence.
>P42857|NSG1
1 MVKLGNNFAE KGTKQPLLED GFDTIPLMTP LDVNQLQFPP PDKVVVKTKT EYEPDRKKGK
61 ARPPQIAEFT VSITEGVTER FKVSVLVLFA LAFLTCVVFL VVYKVYKYDR ACPDGFVLKN
121 TQCIPEGLES YYAEQDSSAR EKFYTVINHY NLAKQSITRS VSPWMSVLSE EKLSEQETEA
181 AEKSALocalizationUniProt · AlphaFold · HPA
Whether an antibody against NSG1 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
- Other membrane
- Secreted
- No
- Transmembrane segments
- 1
- Mean surface accessibility (rSASA)
- 0.59
- Highest tissue expression
- 133 nTPM
Expression across tissuesHPA
Tissue
- pituitary gland: 133 nTPM
- skin: 105 nTPM
- cerebellum: 92 nTPM
- hypothalamus: 91 nTPM
- basal ganglia: 76 nTPM
- cerebral cortex: 58 nTPM
Single-cell type
- oocytes: 539 nCPM
- melanocytes: 447 nCPM
- retinal bipolar cells: 344 nCPM
- epididymal efferent duct absorptive cells: 200 nCPM
- corticotrophs: 173 nCPM
- granulosa cells: 168 nCPM
Immune cell
- MAIT T-cell: 59 nTPM
- gdT-cell: 42 nTPM
- memory CD4 T-cell: 38 nTPM
- memory CD8 T-cell: 35 nTPM
- naive CD8 T-cell: 26 nTPM
- total PBMC: 13 nTPM
Brain region
- hypothalamus: 242 nTPM
- midbrain: 155 nTPM
- cerebellum: 148 nTPM
- pons: 144 nTPM
- medulla oblongata: 142 nTPM
- cerebral cortex: 126 nTPM
ReferencesPubMed · IEDB
Publications for NSG1 from three distinct lines of evidence, kept separate because they answer different questions: whether antibodies are directed at the protein, whether a B-cell epitope has been mapped on it, and whether a T-cell epitope has. Each is labelled with its source.
Reference: AutoantibodyPubMed
2 publications
- Development of a panel of autoantibody against NSG1 with CEA, CYFRA21-1, and SCC-Ag for the diagnosis of esophageal squamous cell carcinoma.
2021 · Clin Chim Acta · RCR 2 · 33 citations - Development of a panel of serum IgG and IgA autoantibodies for early diagnosis of colon cancer.
2020 · Int J Med Sci · RCR 0.4 · 9 citations
Sources: PubMed — antigen-level antibody evidence from a custom retrieval. Records matching a controlled set of autoantibody terms (the MeSH descriptors Autoantibodies and Autoantigens, with title and abstract term variants) were obtained through NCBI E-utilities, and their titles and abstracts parsed for constructions that direct an antibody at a named protein rather than for co-occurrence. Captured names were resolved against UniProt nomenclature and each antigen adjudicated individually against the source text. Bibliographic records from PubMed and MeSH, U.S. National Library of Medicine; citation metrics from NIH iCite (Hutchins et al., PLoS Biology 2016). Titles link to PubMed; abstracts are not reproduced here. The NLM does not endorse this analysis.
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)
- 1.29
- gnomAD pLI
- 0.01
- gnomAD missense Z
- -0.37
- DepMap mean gene effect
- 0.14
- 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
- amyloid precursor protein metabolic process
- apoptotic process
- clathrin coat assembly
- endosomal transport
- neurotransmitter receptor transport, endosome to postsynaptic membrane
- positive regulation of receptor recycling
- postsynaptic neurotransmitter receptor cycle
- receptor recycling
- regulation of long-term synaptic potentiation
- spontaneous synaptic transmission
- vesicle-mediated transport in synapse
- neurotransmitter receptor cycle
Molecular functions
Cellular components
- cytoplasm
- dendrite
- early endosome membrane
- endoplasmic reticulum
- endoplasmic reticulum membrane
- endosome
- glutamatergic synapse
- Golgi cisterna membrane
- late endosome
- lateral plasma membrane
- lysosomal lumen
- membrane
- multivesicular body membrane
- nucleus
- postsynaptic endosome
- postsynaptic membrane
- recycling endosome membrane
- somatodendritic compartment
- trans-Golgi network membrane
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NSG1 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 NSG1 as an antibody target. Whether an autoantibody or antibody against NSG1 could matter depends on whether native NSG1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NSG1 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 NSG1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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