CAMKV
CaM kinase-like vesicle-associated protein
Also known as: CAMKV_HUMAN, MGC8407, VACAMKL
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8NCB2
- Gene
- CAMKV
- Ensembl
- ENSG00000164076
- Chromosome
- 3
- Canonical length
- 501 aa
- Protein class
- Enzymes, Predicted intracellular proteins
- Subcellular location
- Nucleoplasm,Cytokinetic bridge
OverviewNCBI Gene
Predicted to enable calcium/calmodulin-dependent protein kinase activity and calmodulin binding activity. Predicted to be involved in signal transduction. Predicted to be located in cytoplasmic vesicle membrane and plasma membrane. Predicted to be active in cytoplasm; glutamatergic synapse; and postsynapse. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
501 residues, UniProt reviewed canonical sequence.
>Q8NCB2|CAMKV
1 MPFGCVTLGD KKNYNQPSEV TDRYDLGQVI KTEEFCEIFR AKDKTTGKLH TCKKFQKRDG
61 RKVRKAAKNE IGILKMVKHP NILQLVDVFV TRKEYFIFLE LATGREVFDW ILDQGYYSER
121 DTSNVVRQVL EAVAYLHSLK IVHRNLKLEN LVYYNRLKNS KIVISDFHLA KLENGLIKEP
181 CGTPEYLAPE VVGRQRYGRP VDCWAIGVIM YILLSGNPPF YEEVEEDDYE NHDKNLFRKI
241 LAGDYEFDSP YWDDISQAAK DLVTRLMEVE QDQRITAEEA ISHEWISGNA ASDKNIKDGV
301 CAQIEKNFAR AKWKKAVRVT TLMKRLRAPE QSSTAAAQSA SATDTATPGA AGGATAAAAS
361 GATSAPEGDA ARAAKSDNVA PADRSATPAT DGSATPATDG SVTPATDGSI TPATDGSVTP
421 ATDRSATPAT DGRATPATEE STVPTTQSSA MLATKAAATP EPAMAQPDST APEGATGQAP
481 PSSKGEEAAG YAQESQREEA SLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CAMKV 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)
- 0.43
- Highest tissue expression
- 220 nTPM
Expression across tissuesHPA
Tissue
- basal ganglia: 220 nTPM
- cerebral cortex: 113 nTPM
- hippocampal formation: 86 nTPM
- amygdala: 66 nTPM
- hypothalamus: 45 nTPM
- midbrain: 10 nTPM
Single-cell type
- brain inhibitory neurons: 85 nCPM
- brain excitatory neurons: 46 nCPM
- retinal amacrine cells: 42 nCPM
- other brain neurons: 36 nCPM
- late spermatids: 15 nCPM
- oligodendrocytes: 7.7 nCPM
Immune cell
- neutrophil: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- basal ganglia: 235 nTPM
- cerebral cortex: 218 nTPM
- hippocampal formation: 192 nTPM
- amygdala: 132 nTPM
- white matter: 122 nTPM
- thalamus: 121 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)
- 0.22
- gnomAD pLI
- 1
- gnomAD missense Z
- 3.32
- DepMap mean gene effect
- -0.1
- DepMap dependency class
- selective
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
- modulation of chemical synaptic transmission
- regulation of modification of postsynaptic structure
- signal transduction
Molecular functions
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CAMKV 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 CAMKV as an antibody target. Whether an autoantibody or antibody against CAMKV could matter depends on whether native CAMKV is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CAMKV is annotated at the cell surface, where native CAMKV 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 CAMKV as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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