CLEC3B
Tetranectin
Also known as: TETN_HUMAN, TN, TNA
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- P05452
- Gene
- CLEC3B
- Ensembl
- ENSG00000163815
- Chromosome
- 3
- Canonical length
- 202 aa
- Protein class
- Cancer-related genes, Disease related genes, Plasma proteins, Predicted intracellular proteins, Predicted secreted proteins
- Secretome location
- Secreted to blood
- Quaternary structure
- Homotrimer
OverviewNCBI Gene
Enables calcium ion binding activity; heparin binding activity; and kringle domain binding activity. Involved in bone mineralization. Located in cytoplasm; extracellular space; and granular component. Implicated in osteoarthritis and retinal macular dystrophy 4. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
202 residues, UniProt reviewed canonical sequence.
>P05452|CLEC3B
1 MELWGAYLLL CLFSLLTQVT TEPPTQKPKK IVNAKKDVVN TKMFEELKSR LDTLAQEVAL
61 LKEQQALQTV CLKGTKVHMK CFLAFTQTKT FHEASEDCIS RGGTLGTPQT GSENDALYEY
121 LRQSVGNEAE IWLGLNDMAA EGTWVDMTGA RIAYKNWETE ITAQPDGGKT ENCAVLSGAA
181 NGKWFDKRCR DQLPYICQFG IVLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLEC3B 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)
- 0.38
- Highest tissue expression
- 461 nTPM
Expression across tissuesHPA
Tissue
- adipose tissue: 461 nTPM
- heart muscle: 298 nTPM
- spleen: 268 nTPM
- breast: 243 nTPM
- lung: 225 nTPM
- skin: 166 nTPM
Single-cell type
- ependymal cells: 121 nCPM
- vascular endothelial cells: 37 nCPM
- late spermatids: 29 nCPM
- fibroblasts: 27 nCPM
- leydig cells: 15 nCPM
- epididymal clear cells: 12 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
- midbrain: 53 nTPM
- medulla oblongata: 45 nTPM
- choroid plexus: 42 nTPM
- thalamus: 41 nTPM
- cerebral cortex: 35 nTPM
- pons: 34 nTPM
DiseaseUniProt · ClinVar · IEDB · PubMed
Four sources answering four different questions about CLEC3B.
Disease | AllUniProt
Conditions CLEC3B is implicated in, by any mechanism.
- Macular dystrophy, retinal, 4 (MCDR4) MIM:619977
Disease | GeneticClinVar
1 pathogenic / likely-pathogenic of 28 ClinVar records.
Conditions with pathogenic or likely-pathogenic variants.
- Macular dystrophy, retinal, 4
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)
- 1.34
- gnomAD pLI
- 0
- gnomAD missense Z
- 1.33
- DepMap mean gene effect
- -0.03
- 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
Molecular functions
- calcium ion binding
- carbohydrate binding
- heparin binding
- kringle domain binding
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CLEC3B as an antibody target. Whether an autoantibody or antibody against CLEC3B could matter depends on whether native CLEC3B is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLEC3B is annotated as secreted, so native CLEC3B 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 CLEC3B as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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