CBLN2
Cerebellin-2
Also known as: CBLN2_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q8IUK8
- Gene
- CBLN2
- Ensembl
- ENSG00000141668
- Chromosome
- 18
- Canonical length
- 224 aa
- Protein class
- Predicted intracellular proteins, Predicted secreted proteins
- Subcellular location
- Cytosol,Perinuclear theca,Calyx,Flagellar centriole,Mid piece,Principal piece
- Secretome location
- Secreted in brain
- Quaternary structure
- Homohexamer
OverviewNCBI Gene
Predicted to be involved in maintenance of synapse structure and spontaneous synaptic transmission. Predicted to act upstream of or within positive regulation of synapse assembly. Predicted to be located in synaptic cleft. Predicted to be part of trans-synaptic protein complex. Predicted to be active in glutamatergic synapse. [provided by Alliance of Genome Resources, Apr 2025]
Canonical amino-acid sequenceUniProt
224 residues, UniProt reviewed canonical sequence.
>Q8IUK8|CBLN2
1 MQAPGRGPLG LRLMMPGRRG ALREPGGCGS CLGVALALLL LLLPACCPVR AQNDTEPIVL
61 EGKCLVVCDS SPSADGAVTS SLGISVRSGS AKVAFSATRS TNHEPSEMSN RTMTIYFDQV
121 LVNIGNHFDL ASSIFVAPRK GIYSFSFHVV KVYNRQTIQV SLMQNGYPVI SAFAGDQDVT
181 REAASNGVLL LMEREDKVHL KLERGNLMGG WKYSTFSGFL VFPLLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CBLN2 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
- Secreted
- Secreted
- Yes
- Transmembrane segments
- 0
- Mean surface accessibility (rSASA)
- 0.45
- Highest tissue expression
- 38 nTPM
Expression across tissuesHPA
Tissue
- cerebral cortex: 38 nTPM
- hypothalamus: 8.4 nTPM
- midbrain: 5.3 nTPM
- amygdala: 5.2 nTPM
- seminal vesicle: 4.8 nTPM
- retina: 4.7 nTPM
Single-cell type
- brain excitatory neurons: 121 nCPM
- mesothelial cells: 35 nCPM
- epicardial cells: 23 nCPM
- retinal amacrine cells: 18 nCPM
- neuroendocrine cells: 14 nCPM
- somatotrophs: 9 nCPM
Immune cell
- naive B-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
- eosinophil: 0 nTPM
- gdT-cell: 0 nTPM
- intermediate monocyte: 0 nTPM
Brain region
- cerebral cortex: 108 nTPM
- white matter: 64 nTPM
- basal ganglia: 53 nTPM
- pons: 53 nTPM
- thalamus: 48 nTPM
- midbrain: 38 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)
- 1.17
- gnomAD pLI
- 0.12
- gnomAD missense Z
- 1.87
- DepMap mean gene effect
- -0.06
- DepMap dependency class
- selective
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
- maintenance of synapse structure
- positive regulation of synapse assembly
- spontaneous synaptic transmission
- synapse assembly
- synapse organization
- trans-synaptic signaling, modulating synaptic transmission
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of CBLN2 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 CBLN2 as an antibody target. Whether an autoantibody or antibody against CBLN2 could matter depends on whether native CBLN2 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CBLN2 is annotated as secreted, so native CBLN2 circulates and is directly accessible to antibodies. Secreted and cell-surface proteins are the autoantibody targets most likely to act like drugs, blocking or depleting the native protein.
Annotation status
The present source text does not explicitly label CBLN2 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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