CLEC9A
C-type lectin domain family 9 member A
Also known as: CD370, CLC9A_HUMAN, DNGR-1, HEEE9341, UNQ9341
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q6UXN8
- Gene
- CLEC9A
- Ensembl
- ENSG00000197992
- Chromosome
- 12
- Canonical length
- 241 aa
- Protein class
- CD markers, Predicted membrane proteins
- Quaternary structure
- Homodimer
OverviewNCBI Gene
CLEC9A is a group V C-type lectin-like receptor (CTLR) that functions as an activation receptor and is expressed on myeloid lineage cells (Huysamen et al., 2008 [PubMed 18408006]).[supplied by OMIM, Aug 2008]
Canonical amino-acid sequenceUniProt
241 residues, UniProt reviewed canonical sequence.
>Q6UXN8|CLEC9A
1 MHEEEIYTSL QWDSPAPDTY QKCLSSNKCS GACCLVMVIS CVFCMGLLTA SIFLGVKLLQ
61 VSTIAMQQQE KLIQQERALL NFTEWKRSCA LQMKYCQAFM QNSLSSAHNS SPCPNNWIQN
121 RESCYYVSEI WSIWHTSQEN CLKEGSTLLQ IESKEEMDFI TGSLRKIKGS YDYWVGLSQD
181 GHSGRWLWQD GSSPSPGLLP AERSQSANQV CGYVKSNSLL SSNCSTWKYF ICEKYALRSS
241 VLocalizationUniProt · AlphaFold · HPA
Whether an antibody against CLEC9A 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)
- 0.41
- Highest tissue expression
- 7 nTPM
Expression across tissuesHPA
Tissue
- lymph node: 7 nTPM
- thymus: 4.6 nTPM
- spleen: 4.5 nTPM
- spinal cord: 4.1 nTPM
- midbrain: 2.9 nTPM
- testis: 2.8 nTPM
Single-cell type
- microglia: 114 nCPM
- cdc: 88 nCPM
- hematopoietic stem cells: 50 nCPM
- macrophages: 20 nCPM
- late primary spermatocytes: 15 nCPM
- early primary spermatocytes: 11 nCPM
Immune cell
- myeloid DC: 22 nTPM
- neutrophil: 7.9 nTPM
- total PBMC: 0.4 nTPM
- NK-cell: 0.1 nTPM
- basophil: 0 nTPM
- classical monocyte: 0 nTPM
Brain region
- medulla oblongata: 4.4 nTPM
- white matter: 4 nTPM
- spinal cord: 3.4 nTPM
- hypothalamus: 3 nTPM
- cerebellum: 2.9 nTPM
- pons: 2.9 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)
- 1.21
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.5
- DepMap mean gene effect
- 0.09
- DepMap dependency class
- none
Cancer expressionTCGA
Across TCGA tumor cohorts, this protein is over-expressed in roughly 4% 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 CLEC9A as an antibody target. Whether an autoantibody or antibody against CLEC9A could matter depends on whether native CLEC9A is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
CLEC9A is annotated at the cell surface, where native CLEC9A 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 CLEC9A as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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