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 QPLLSLDLocalizationUniProt · 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.
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