SIGLEC5
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Also known as OB-BP2SIGLEC-5CD170
Summary
SIGLEC5 (sialic acid binding Ig like lectin 5, HGNC:10874) is a long non-coding RNA gene on chromosome 19q13.41. Putative adhesion molecule that mediates sialic-acid dependent binding to cells.
This gene encodes a member of the sialic acid-binding immunoglobulin-like lectin (Siglec) family. These cell surface lectins are characterized by structural motifs in the immunoglobulin (Ig)-like domains and sialic acid recognition sites in the first Ig V set domain. The encoded protein is a member of the CD33-related subset of Siglecs and inhibits the activation of several cell types including monocytes, macrophages and neutrophils. Binding of group B Streptococcus (GBS) to the encoded protein plays a role in GBS immune evasion.
Source: NCBI Gene 8778 — RefSeq curated summary.
At a glance
- Gene type: non-coding (lncRNA) — no protein product; not a drug target. Variant/disease associations are omitted (they would be positional, from an overlapping protein-coding gene).
- Dosage sensitivity (ClinGen): haploinsufficiency dosage sensitivity unlikely, triplosensitivity no evidence
Identifiers
Gene identifiers
| Field | Value |
|---|---|
| HGNC ID | HGNC:10874 |
| Approved symbol | SIGLEC5 |
| Name | sialic acid binding Ig like lectin 5 |
| Location | 19q13.41 |
| Locus type | gene with protein product |
| Status | Approved |
| Aliases | OB-BP2, SIGLEC-5, CD170 |
| Ensembl gene | ENSG00000105501 |
| Ensembl biotype | lncRNA |
| OMIM | 604200 |
| Entrez | 8778 |
Gene structure
Transcript identifiers
Ensembl transcripts: 1 — 1 lncRNA
ENST00000534261
RefSeq mRNA: 0 — MANE Select: None
Canonical transcript exons
ENST00000534261 — 3 exons
| Exon | Start | End |
|---|---|---|
| ENSE00002156182 | 51630299 | 51630666 |
| ENSE00002188877 | 51645477 | 51645545 |
| ENSE00003475926 | 51630101 | 51630216 |
Expression profiles
Bgee: expression breadth ubiquitous, 120 present calls, max score 93.38.
Top tissues by expression
130 total, by Bgee expression score (0-100, higher = more expressed):
| Tissue | Anatomy ID | Expression score | Quality |
|---|---|---|---|
| blood | UBERON:0000178 | 93.38 | gold quality |
| male germ line stem cell (sensu Vertebrata) in testis | CL:0000089 ∩ UBERON:0000473 | 87.10 | gold quality |
| leukocyte | CL:0000738 | 85.42 | gold quality |
| monocyte | CL:0000576 | 85.41 | gold quality |
| granulocyte | CL:0000094 | 83.10 | gold quality |
| spleen | UBERON:0002106 | 79.85 | gold quality |
| bone marrow | UBERON:0002371 | 77.98 | gold quality |
| bone marrow cell | CL:0002092 | 74.15 | gold quality |
| vermiform appendix | UBERON:0001154 | 74.15 | gold quality |
| lymph node | UBERON:0000029 | 70.53 | gold quality |
| right lung | UBERON:0002167 | 67.66 | gold quality |
| upper lobe of left lung | UBERON:0008952 | 64.12 | gold quality |
| placenta | UBERON:0001987 | 63.58 | gold quality |
| smooth muscle tissue | UBERON:0001135 | 62.76 | gold quality |
| apex of heart | UBERON:0002098 | 59.42 | gold quality |
| small intestine Peyer’s patch | UBERON:0003454 | 59.26 | gold quality |
| lung | UBERON:0002048 | 59.19 | gold quality |
| rectum | UBERON:0001052 | 57.78 | gold quality |
| gall bladder | UBERON:0002110 | 57.13 | gold quality |
| small intestine | UBERON:0002108 | 56.56 | gold quality |
| omental fat pad | UBERON:0010414 | 55.19 | gold quality |
| descending thoracic aorta | UBERON:0002345 | 54.23 | gold quality |
| C1 segment of cervical spinal cord | UBERON:0006469 | 52.67 | gold quality |
| mucosa of transverse colon | UBERON:0004991 | 51.54 | gold quality |
| left uterine tube | UBERON:0001303 | 51.30 | gold quality |
| adipose tissue | UBERON:0001013 | 50.91 | gold quality |
| right lobe of liver | UBERON:0001114 | 50.49 | gold quality |
| right coronary artery | UBERON:0001625 | 50.47 | gold quality |
| hindlimb stylopod muscle | UBERON:0004252 | 50.43 | gold quality |
| putamen | UBERON:0001874 | 50.12 | gold quality |
Single-cell (SCXA)
Detected in 1 experiment(s), a significant marker in 0.
| Experiment | Marker? | Max mean expression |
|---|---|---|
| E-ANND-3 | no | 2.00 |
Regulation
Is transcription factor: no
miRNA regulators (miRDB)
43 targeting SIGLEC5, top 30 by miRDB confidence (max_score; target_count = how many genes the miRNA targets in total — lower means more specific):
| miRNA | Max score | Avg score | miRNA target_count |
|---|---|---|---|
| HSA-MIR-4533 | 100.00 | 69.48 | 2758 |
| HSA-MIR-4747-5P | 100.00 | 67.90 | 2681 |
| HSA-MIR-5196-5P | 100.00 | 67.98 | 2761 |
| HSA-MIR-3064-3P | 100.00 | 70.09 | 1254 |
| HSA-MIR-3646 | 100.00 | 73.56 | 5283 |
| HSA-MIR-4500 | 99.99 | 72.72 | 2367 |
| HSA-LET-7A-5P | 99.98 | 72.29 | 1790 |
| HSA-LET-7B-5P | 99.98 | 72.31 | 1790 |
| HSA-LET-7C-5P | 99.98 | 72.29 | 1790 |
| HSA-LET-7E-5P | 99.98 | 72.29 | 1790 |
| HSA-LET-7F-5P | 99.98 | 72.56 | 1784 |
| HSA-LET-7G-5P | 99.98 | 72.37 | 1784 |
| HSA-LET-7I-5P | 99.98 | 72.37 | 1788 |
| HSA-MIR-98-5P | 99.98 | 72.33 | 1787 |
| HSA-MIR-4482-3P | 99.98 | 72.50 | 3147 |
| HSA-LET-7D-5P | 99.96 | 71.76 | 1632 |
| HSA-MIR-4458 | 99.96 | 71.64 | 1650 |
| HSA-MIR-6721-5P | 99.93 | 68.92 | 2981 |
| HSA-MIR-202-3P | 99.84 | 71.41 | 1290 |
| HSA-MIR-3679-3P | 99.64 | 69.88 | 1599 |
| HSA-MIR-5003-5P | 99.61 | 69.13 | 1624 |
| HSA-MIR-3128 | 99.50 | 67.85 | 1258 |
| HSA-MIR-302A-5P | 99.39 | 68.21 | 1913 |
| HSA-MIR-361-3P | 99.19 | 66.45 | 1381 |
| HSA-MIR-6809-5P | 99.13 | 68.45 | 1223 |
| HSA-MIR-29A-5P | 99.08 | 68.59 | 1813 |
| HSA-MIR-3124-3P | 98.87 | 68.95 | 2123 |
| HSA-MIR-5006-5P | 98.79 | 66.92 | 1246 |
| HSA-MIR-4755-3P | 98.77 | 65.59 | 1915 |
| HSA-MIR-4317 | 98.49 | 67.09 | 987 |
Functional genomics
ClinGen dosage: haploinsufficiency 40 (dosage sensitivity unlikely), triplosensitivity 0 (no evidence). ClinGen Gene Dosage Map
Literature-anchored findings (GeneRIF, showing 25)
- expression of Siglec-5 on cells of the myelomonocytic lineage and alteration of its expression by inflammatory stimuli suggest a role for this protein in cell/cell interactions following microbial exposure. (PMID:12763136)
- Siglec-5 can be classified as an inhibitory receptor with the potential to mediate SHP-1 and/or SHP-2-dependent signaling in the absence of tyrosine phosphorylation. (PMID:15769739)
- Siglecs-5 did not interact with sulfate derivatives of LacNAc and sulfated oligosaccharides containing sialic acid. (PMID:16732727)
- The expression levels of Siglec-5 were high or detectable in bone marrow plasma from AML patients and serum from normal donors. (PMID:16828866)
- Siglec-14 and Siglec-5 appear to be the first glycan binding paired receptors. Near-complete sequence identity of the amino-terminal part of human Siglec-14 and Siglec-5 indicates partial gene conversion between SIGLEC14 and SIGLEC5. (PMID:17012248)
- Siglec-5 is identified as a receptor for alpha-1-acid glycoprotein (AGP) 1 in human neutrophils. (PMID:17675532)
- Structural implications of SIGLEC5-mediated sialoglycan recognition are reported. (PMID:18022638)
- Group B Streptococcus beta protein binding to Siglec-5 functions to impair leukocyte phagocytosis, oxidative burst, and extracellular trap production, promoting bacterial survival. (PMID:19596804)
- Siglec-5 expression correlates with lack of proliferation in a subset of human cells, and is upregulated by activation of chimpanzee but not human lymphocytes. (PMID:20231688)
- Human Siglec-5 inhibitory receptor and immunoglobulin A (IgA) have separate binding sites in streptococcal beta protein. (PMID:21795693)
- Siglec-5 expression protects T cells from HIV-1- and apoptosis-induced cell death and contributes to the different outcomes of HIV-1 infection in humans and chimpanzees. (PMID:22945238)
- These studies demonstrate the Siglec5 carbohydrate recognition domain alone is sufficient for binding sialylated carbohydrates and provide a foundation for further investigation of Siglec5 structure and function. (PMID:23321067)
- we found that secretory IgA is taken up by M cells via the Dectin-1 receptor, with the possible involvement of Siglec-5 acting as a co-receptor. (PMID:24068891)
- Data indicate that the Siglec-5/14 genotype influences neutrophil responses to group B Streptococcus. (PMID:24799499)
- An unbiased screen revealed Hsp70 as a ligand for Siglec-5 and Siglec-14. Hsp70 stimulation through Siglec-5 delivers an anti-inflammatory signal, while stimulation through Siglec-14 is pro-inflammatory. (PMID:26459514)
- PSGL1 and Siglec-5 are in close proximity at the leukocyte surface.SPSGL1 is a ligand for Siglec-5 and interacts with Siglec-5 ectodomain.Siglec-5 plays a role in PSGL1-mediated leukocyte rolling and the inflammatory response in general. (PMID:27892504)
- Plasma Siglec-5 levels are implicated as an early diagnostic marker of CLI in T2DM patients and it may become a target for the prevention or treatment of CLI in diabetes. (PMID:28900239)
- Genetic susceptibility of common polymorphisms in NIN and SIGLEC5 to chronic periodontitis. (PMID:30765789)
- Soluble siglec-5 is a novel salivary biomarker for primary Sjogren’s syndrome. (PMID:30922727)
- Periodontitis Risk Variants at SIGLEC5 Impair ERG and MAFB Binding. (PMID:34852650)
- Siglec-5 is an inhibitory immune checkpoint molecule for human T cells. (PMID:35290663)
- Siglec-5 and Siglec-14 mediate the endocytosis of ADAMTS13. (PMID:36116391)
- Case-only design identifies interactions of genetic risk variants at SIGLEC5 and PLG with the lncRNA CTD-2353F22.1 implying the importance of periodontal wound healing for disease aetiology. (PMID:36129033)
- PSGL-1: a novel immune checkpoint driving T-cell dysfunction in obstructive sleep apnea. (PMID:37854605)
- The prognostic impact of SIGLEC5-induced impairment of CD8[+] T cell activation in sepsis. (PMID:37890368)
Cross-species orthologs
0 orthologs
Protein
Non-coding RNA — no protein product; not a drug target.
Function
No curated pathway, Gene-Ontology, or interaction data.
Disease & clinical
No curated disease, variant, or cancer-driver associations.
Drugs & pharmacology
No drug or pharmacology data — not an established drug target.
Related Atlas pages
- Disease cohort memberships (association, not causation — diseases whose associated-gene cohort lists this gene; a subset are also under Associated diseases): leprosy, periodontitis, periodontitis, aggressive 1, systemic lupus erythematosus