Seroatlas · Human Serome Atlas

CLVS2

Clavesin-2

Also known as: bA160A10.4, C6orf212, C6orf213, CLVS2_HUMAN, RLBP1L2

Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene

Protein identityUniProt · HPA

UniProt accession
Q5SYC1
Gene
CLVS2
Ensembl
ENSG00000146352
Chromosome
6
Canonical length
327 aa
Protein class
Predicted intracellular proteins

OverviewNCBI Gene

This gene encodes a protein that belongs to the SEC14/CRAL-TRIO family of proteins. A similar protein in rat is thought to function in the endosomal pathway between early endosomes and mature lysosomes. [provided by RefSeq, Aug 2013]

Canonical amino-acid sequenceUniProt

327 residues, UniProt reviewed canonical sequence.

>Q5SYC1|CLVS2
     1  MTHLQAGLSP ETLEKARLEL NENPDTLHQD IQEVRDMVIT RPDIGFLRTD DAFILRFLRA
    61  RKFHHFEAFR LLAQYFEYRQ QNLDMFKSFK ATDPGIKQAL KDGFPGGLAN LDHYGRKILV
   121  LFAANWDQSR YTLVDILRAI LLSLEAMIED PELQVNGFVL IIDWSNFTFK QASKLTPSML
   181  RLAIEGLQDS FPARFGGIHF VNQPWYIHAL YTVIRPFLKE KTRKRIFLHG NNLNSLHQLI
   241  HPEILPSEFG GMLPPYDMGT WARTLLDHEY DDDSEYNVDS YSMPVKEVEK ELSPKSMKRS
   301  QSVVDPTVLK RMDKNEEENM QPLLSLD

LocalizationUniProt · AlphaFold · HPA

Whether an antibody against CLVS2 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
0
Mean surface accessibility (rSASA)
0.32
Highest tissue expression
17 nTPM

Expression across tissuesHPA

Tissue

  • cerebellum: 17 nTPM
  • cerebral cortex: 8.6 nTPM
  • retina: 7.6 nTPM
  • basal ganglia: 3.8 nTPM
  • prostate: 2.8 nTPM
  • hippocampal formation: 2.7 nTPM

Single-cell type

  • corticotrophs: 222 nCPM
  • brain excitatory neurons: 181 nCPM
  • müller glia: 153 nCPM
  • brain inhibitory neurons: 140 nCPM
  • retinal ganglion cells: 124 nCPM
  • gonadotrophs: 94 nCPM

Immune cell

  • basophil: 0 nTPM
  • classical monocyte: 0 nTPM
  • eosinophil: 0 nTPM
  • gdT-cell: 0 nTPM
  • intermediate monocyte: 0 nTPM
  • MAIT T-cell: 0 nTPM

Brain region

  • cerebellum: 113 nTPM
  • cerebral cortex: 46 nTPM
  • hypothalamus: 41 nTPM
  • basal ganglia: 36 nTPM
  • pons: 36 nTPM
  • white matter: 30 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)
0.86
gnomAD pLI
0.01
gnomAD missense Z
1.8
DepMap mean gene effect
0.08
DepMap dependency class
none

Cancer expressionTCGA

Across TCGA tumor cohorts, this protein is over-expressed in roughly 2% of surveyed tumor types (aggregate summary; per-cohort expression, alteration, and survival load in the interactive view).

OntologyGO

Biological processes

Molecular functions

Cellular components

Protein domainsUniProt · Pfam · InterPro

KeywordsUniProt

Antibody and autoantibody relevanceSeroatlas analysis

Seroatlas reads CLVS2 as an antibody target. Whether an autoantibody or antibody against CLVS2 could matter depends on whether native CLVS2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.

CLVS2 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 CLVS2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.

Canonical record: https://seroatlas.com/gene/CLVS2. Study-independent annotations aggregated from UniProt, Human Protein Atlas, PubMed, IEDB, Pfam, InterPro, Gene Ontology, AlphaFold, gnomAD, DepMap, ClinVar, TCGA. Catalog release seroatlas-reviewed-human-uniprot-20260313.

Seroatlas is the reference for exploring autoantibody and antibody serology at the human-protein level: the autoreactome and human serome, multiplex serology (HuProt, HuScan, VirScan, PhIP-Seq).

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