CLEC17A
C-type lectin domain family 17, member A
Also known as: CL17A_HUMAN, FLJ45910
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6ZS10
- Gene
- CLEC17A
- Ensembl
- ENSG00000187912
- Chromosome
- 19
- Canonical length
- 378 aa
- Protein class
- Predicted membrane proteins
OverviewNCBI Gene
Enables D-mannose binding activity; fucose binding activity; and identical protein binding activity. Predicted to be involved in immune response. Located in cell surface. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
378 residues, UniProt reviewed canonical sequence.
>Q6ZS10|CLEC17A
1 MHNLYSITGY PDPPGTMEEE EEDDDYENST PPYKDLPPKP GTMEEEEEDD DYENSTPPYK
61 DLPPKPGTME EEEEDDDYEN STPPYKDLPP KPGSSAPPRP PRAAKETEKP PLPCKPRNMT
121 GLDLAAVTCP PPQLAVNLEP SPLQPSLAAT PVPWLNQRSG GPGCCQKRWM VYLCLLVVTS
181 LFLGCLGLTV TLIKYQELME ELRMLSFQQM TWRTNMTGMA GLAGLKHDIA RVRADTNQSL
241 VELWGLLDCR RITCPEGWLP FEGKCYYFSP STKSWDEARM FCQENYSHLV IINSFAEHNF
301 VAKAHGSPRV YWLGLNDRAQ EGDWRWLDGS PVTLSFWEPE EPNNIHDEDC ATMNKGGTWN
361 DLSCYKTTYW ICERKCSCLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLEC17A 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
- 1
- Mean surface accessibility (rSASA)
- 0.52
- Highest tissue expression
- 17 nTPM
Expression across tissuesHPA
Tissue
- tonsil: 17 nTPM
- lymph node: 15 nTPM
- spleen: 10 nTPM
- appendix: 7.7 nTPM
- small intestine: 5.3 nTPM
- bone marrow: 1.9 nTPM
Single-cell type
- tuft cells: 69 nCPM
- b-cells: 67 nCPM
- microglia: 35 nCPM
- neutrophils: 20 nCPM
- early spermatids: 12 nCPM
- cdc: 9.2 nCPM
Immune cell
- naive B-cell: 43 nTPM
- memory B-cell: 22 nTPM
- myeloid DC: 3 nTPM
- neutrophil: 2.6 nTPM
- total PBMC: 2.2 nTPM
- classical monocyte: 0.7 nTPM
Brain region
- white matter: 6.8 nTPM
- cerebellum: 6.6 nTPM
- medulla oblongata: 6.6 nTPM
- cerebral cortex: 6.2 nTPM
- pons: 6.1 nTPM
- hypothalamus: 5.7 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)
- 0.94
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.88
- DepMap mean gene effect
- 0
- DepMap dependency class
- none
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
- D-mannose binding
- fucose binding
- identical protein binding
- metal ion binding
- pattern recognition receptor activity
Cellular components
Protein domainsUniProt · Pfam · InterPro
KeywordsUniProt
Antibody and autoantibody relevanceSeroatlas analysis
Seroatlas reads CLEC17A as an antibody target. Whether an autoantibody or antibody against CLEC17A could matter depends on whether native CLEC17A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLEC17A is annotated at the cell surface, where native CLEC17A 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 CLEC17A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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