SIGLEC14
Sialic acid-binding Ig-like lectin 14
Also known as: SIG14_HUMAN
Cross-references: UniProt · Ensembl · Human Protein Atlas · GeneCards · NCBI Gene
Protein identityUniProt · HPA
- UniProt accession
- Q08ET2
- Gene
- SIGLEC14
- Ensembl
- ENSG00000254415
- Chromosome
- 19
- Canonical length
- 396 aa
- Protein class
- Plasma proteins, Predicted membrane proteins
- Subcellular location
- Vesicles,Plasma membrane
OverviewNCBI Gene
Predicted to enable sialic acid binding activity. Predicted to be involved in cell adhesion. Predicted to be located in ficolin-1-rich granule membrane and tertiary granule membrane. Predicted to be active in plasma membrane. [provided by Alliance of Genome Resources, Jul 2025]
Canonical amino-acid sequenceUniProt
396 residues, UniProt reviewed canonical sequence.
>Q08ET2|SIGLEC14
1 MLPLLLLPLL WGGSLQEKPV YELQVQKSVT VQEGLCVLVP CSFSYPWRSW YSSPPLYVYW
61 FRDGEIPYYA EVVATNNPDR RVKPETQGRF RLLGDVQKKN CSLSIGDARM EDTGSYFFRV
121 ERGRDVKYSY QQNKLNLEVT ALIEKPDIHF LEPLESGRPT RLSCSLPGSC EAGPPLTFSW
181 TGNALSPLDP ETTRSSELTL TPRPEDHGTN LTCQVKRQGA QVTTERTVQL NVSYAPQNLA
241 ISIFFRNGTG TALRILSNGM SVPIQEGQSL FLACTVDSNP PASLSWFREG KALNPSQTSM
301 SGTLELPNIG AREGGEFTCR VQHPLGSQHL SFILSVQRSS SSCICVTEKQ QGSWPLVLTL
361 IRGALMGAGF LLTYGLTWIY YTRCGGPQQS RAERPGLocalizationUniProt · AlphaFold · HPA
Whether an antibody against SIGLEC14 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)
- 0.36
- Highest tissue expression
- 22 nTPM
Expression across tissuesHPA
Tissue
- bone marrow: 22 nTPM
- spleen: 21 nTPM
- appendix: 12 nTPM
- tonsil: 9.1 nTPM
- lymph node: 8.1 nTPM
- small intestine: 4.4 nTPM
Single-cell type
- neutrophils: 8.9 nCPM
- kupffer cells: 4.1 nCPM
- monocytes: 1.8 nCPM
- macrophages: 1.2 nCPM
- cdc: 1.1 nCPM
- monocyte progenitors: 1 nCPM
Immune cell
- neutrophil: 80 nTPM
- intermediate monocyte: 71 nTPM
- non-classical monocyte: 59 nTPM
- classical monocyte: 58 nTPM
- myeloid DC: 35 nTPM
- total PBMC: 20 nTPM
Brain region
- medulla oblongata: 12 nTPM
- thalamus: 10 nTPM
- pons: 9.8 nTPM
- white matter: 9.5 nTPM
- hypothalamus: 9.2 nTPM
- cerebral cortex: 8.5 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)
- 0.89
- gnomAD pLI
- 0
- gnomAD missense Z
- 0.44
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
- Immunoglobulin/major histocompatibility complex, conserved site
- Immunoglobulin subtype 2
- Immunoglobulin domain subtype
- Immunoglobulin-like domain
- Immunoglobulin V-set domain
- CD80-like, immunoglobulin C2-set
- Immunoglobulin-like fold
- Immunoglobulin-like domain superfamily
- Sialic acid-binding Ig-like lectin
- Immunoglobulin V-set domain
- CD80-like C2-set immunoglobulin domain
- Immunoglobulin domain
KeywordsUniProt
InteractionsUniProt · HPA
Protein binding partners of SIGLEC14 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 SIGLEC14 as an antibody target. Whether an autoantibody or antibody against SIGLEC14 could matter depends on whether native SIGLEC14 is physically reachable, whether the body needs it intact, and whether it acts in a disease-relevant tissue.
SIGLEC14 is annotated at the cell surface, where native SIGLEC14 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 SIGLEC14 as an autoantigen. Seroatlas presents hypothesis context only and does not manufacture a known-serology claim.
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