NECAB2
N-terminal EF-hand calcium-binding protein 2
Also known as: EFCBP2, NECA2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q7Z6G3
- Gene
- NECAB2
- Ensembl
- ENSG00000103154
- Chromosome
- 16
- Canonical length
- 386 aa
- Protein class
- Predicted intracellular proteins
OverviewNCBI Gene
The protein encoded by this gene is a neuronal calcium-binding protein that binds to and modulates the function of at least two receptors, adenosine A(2A) receptor and metabotropic glutamate receptor type 5. [provided by RefSeq, Jul 2016]
Canonical amino-acid sequenceUniProt
386 residues, UniProt reviewed canonical sequence.
>Q7Z6G3|NECAB2
1 MCERAARLCR AGAHRLLREP PQQGRALGGL LRWVGARMGE PRESLAPAAP ADPGPASPRG
61 GTAVILDIFR RADKNDDGKL SLEEFQLFFA DGVLNEKELE DLFHTIDSDN TNHVDTKELC
121 DYFVDHMGDY EDVLASLETL NHSVLKAMGY TKKVYEGGSN VDQFVTRFLL KETANQIQSL
181 LSSVESAVEA IEEQTSQLRQ NHIKPSHSAA QTWCGSPTPA SAPNHKLMAM EQGKTLPSAT
241 EDAKEEGLEA QISRLAELIG RLESKALWFD LQQRLSDEDG TNMHLQLVRQ EMAVCPEQLS
301 EFLDSLRQYL RGTTGVRNCF HITAVRLSDG FTFVIYEFWE TEEAWKRHLQ SPLCKAFRHV
361 KVDTLSQPEA LSRILVPAAW CTVGRDLocalizationUniProt · AlphaFold · HPA
Whether an antibody against NECAB2 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)
- 0.45
- Highest tissue expression
- 137 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 137 nTPM
- amygdala: 126 nTPM
- cerebral cortex: 97 nTPM
- hypothalamus: 77 nTPM
- hippocampal formation: 39 nTPM
- choroid plexus: 29 nTPM
Single-cell type
- late spermatids: 82 nCPM
- other brain neurons: 41 nCPM
- brain inhibitory neurons: 36 nCPM
- oocytes: 28 nCPM
- hepatocytes: 23 nCPM
- neutrophils: 20 nCPM
Immune cell
- neutrophil: 56 nTPM
- classical monocyte: 0.8 nTPM
- total PBMC: 0.1 nTPM
- basophil: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
Brain region
- cerebral cortex: 160 nTPM
- pons: 140 nTPM
- basal ganglia: 120 nTPM
- amygdala: 110 nTPM
- hypothalamus: 98 nTPM
- midbrain: 76 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)
- 1.39
- gnomAD pLI
- 0
- gnomAD missense Z
- -4.91
- DepMap mean gene effect
- 0.12
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 3% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).
OntologyGO
Biological processes
- negative regulation of G protein-coupled receptor internalization
- positive regulation of adenosine receptor signaling pathway
- positive regulation of ERK1 and ERK2 cascade
- positive regulation of glutamate receptor signaling pathway
- positive regulation of protein localization to membrane
- regulation of amyloid precursor protein biosynthetic process
Molecular functions
- A2A adenosine receptor binding
- calcium ion binding
- identical protein binding
- type 5 metabotropic glutamate receptor binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of NECAB2 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 NECAB2 as an antibody target. Whether an autoantibody or antibody against NECAB2 could matter depends on whether native NECAB2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
NECAB2 is annotated at the cell surface, where native NECAB2 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 NECAB2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
Loading the interactive Seroatlas protein explorer...