NCS1
Neuronal calcium sensor 1
Also known as: FREQ, NCS-1, NCS1_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P62166
- Gene
- NCS1
- Ensembl
- ENSG00000107130
- Chromosome
- 9
- Canonical length
- 190 aa
- Protein class
- Predicted intracellular proteins
- Subcellular location
- Vesicles,Plasma membrane
OverviewNCBI Gene
This gene is a member of the neuronal calcium sensor gene family, which encode calcium-binding proteins expressed predominantly in neurons. The protein encoded by this gene regulates G protein-coupled receptor phosphorylation in a calcium-dependent manner and can substitute for calmodulin. The protein is associated with secretory granules and modulates synaptic transmission and synaptic plasticity. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
190 residues, UniProt reviewed canonical sequence.
>P62166|NCS1
1 MGKSNSKLKP EVVEELTRKT YFTEKEVQQW YKGFIKDCPS GQLDAAGFQK IYKQFFPFGD
61 PTKFATFVFN VFDENKDGRI EFSEFIQALS VTSRGTLDEK LRWAFKLYDL DNDGYITRNE
121 MLDIVDAIYQ MVGNTVELPE EENTPEKRVD RIFAMMDKNA DGKLTLQEFQ EGSKADPSIV
181 QALSLYDGLVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NCS1 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)
- 0.31
- Highest tissue expression
- 357 nTPM
Expression across tissuesHPA
Tissue
- hippocampal formation: 357 nTPM
- cerebral cortex: 325 nTPM
- amygdala: 320 nTPM
- basal ganglia: 227 nTPM
- colon: 112 nTPM
- hypothalamus: 105 nTPM
Single-cell type
- smooth muscle cells: 151 nCPM
- retinal horizontal cells: 70 nCPM
- retinal amacrine cells: 69 nCPM
- vascular smooth muscle cells: 66 nCPM
- proximal tubule cells: 65 nCPM
- brain excitatory neurons: 63 nCPM
Immune cell
- gdT-cell: 0.1 nTPM
- MAIT T-cell: 0.1 nTPM
- memory CD8 T-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
Brain region
- hippocampal formation: 822 nTPM
- cerebral cortex: 727 nTPM
- amygdala: 640 nTPM
- white matter: 423 nTPM
- basal ganglia: 417 nTPM
- thalamus: 414 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)
- 0.52
- gnomAD pLI
- 0.66
- gnomAD missense Z
- 2.22
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
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
Biological processes
Molecular functions
- calcium ion binding
- calcium sensitive guanylate cyclase activator activity
- voltage-gated calcium channel activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NCS1 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 NCS1 as an antibody target. Whether an autoantibody or antibody against NCS1 could matter depends on whether native NCS1 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NCS1 is annotated at the cell surface, where native NCS1 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 NCS1 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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