NCALD
Neurocalcin-delta
Also known as: NCALD_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P61601
- Gene
- NCALD
- Ensembl
- ENSG00000104490
- Chromosome
- 8
- Canonical length
- 193 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
This gene encodes a member of the neuronal calcium sensor (NCS) family of calcium-binding proteins. The protein contains an N-terminal myristoylation signal and four EF-hand calcium binding loops. The protein is cytosolic at resting calcium levels; however, elevated intracellular calcium levels induce a conformational change that exposes the myristoyl group, resulting in protein association with membranes and partial co-localization with the perinuclear trans-golgi network. The protein is thought to be a regulator of G protein-coupled receptor signal transduction. Several alternatively spliced variants of this gene have been determined, all of which encode the same protein; additional variants may exist but their biological validity has not been determined. [provided by RefSeq, Jul 2008]
Canonical amino-acid sequenceUniProt
193 residues, UniProt reviewed canonical sequence.
>P61601|NCALD
1 MGKQNSKLRP EVMQDLLEST DFTEHEIQEW YKGFLRDCPS GHLSMEEFKK IYGNFFPYGD
61 ASKFAEHVFR TFDANGDGTI DFREFIIALS VTSRGKLEQK LKWAFSMYDL DGNGYISKAE
121 MLEIVQAIYK MVSSVMKMPE DESTPEKRTE KIFRQMDTNR DGKLSLEEFI RGAKSDPSIV
181 RLLQCDPSSA GQFLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NCALD 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)
- 0.3
- Highest tissue expression
- 113 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 113 nTPM
- salivary gland: 95 nTPM
- hippocampal formation: 45 nTPM
- amygdala: 41 nTPM
- breast: 41 nTPM
- ovary: 41 nTPM
Single-cell type
- salivary acinar cells: 1,129 nCPM
- salivary ionocytes: 903 nCPM
- thyrotrophs: 870 nCPM
- respiratory ionocytes: 775 nCPM
- lacrimal acinar cells: 653 nCPM
- nk-cells: 627 nCPM
Immune cell
- NK-cell: 87 nTPM
- gdT-cell: 42 nTPM
- MAIT T-cell: 37 nTPM
- memory CD8 T-cell: 25 nTPM
- naive CD8 T-cell: 21 nTPM
- T-reg: 17 nTPM
Brain region
- cerebral cortex: 183 nTPM
- hippocampal formation: 134 nTPM
- basal ganglia: 121 nTPM
- thalamus: 115 nTPM
- white matter: 97 nTPM
- pons: 87 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)
- 0.41
- gnomAD pLI
- 0.89
- gnomAD missense Z
- 1.56
- DepMap mean gene effect
- -0.04
- 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
Biological processes
- calcium-mediated signaling
- regulation of signal transduction
- regulation of systemic arterial blood pressure
- vesicle-mediated transport
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NCALD 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 NCALD as an antibody target. Whether an autoantibody or antibody against NCALD could matter depends on whether native NCALD is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NCALD 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 NCALD as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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