SIGLEC5 - sialic acid binding Ig like lectin 5 Gene
Also Known as CD170; OBBP2; CD33L2; OB-BP2; SIGLEC-5
Species: Homo sapiens
About SIGLEC5
This gene has 1 transcript (splice variant), 139 orthologues and 16 paralogues. Biased expression in bone marrow (RPKM 12.5), spleen (RPKM 10.6) and 12 other tissues.
Summary
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. [provided by RefSeq, Feb 2012]
SIGLEC5 Products (3)
| mRNA | Protein | Name |
|---|---|---|
| NM_001384708.1 | NP_001371637.1 | sialic acid-binding Ig-like lectin 5 isoform 2 precursor |
| NM_001384709.1 | NP_001371638.1 | sialic acid-binding Ig-like lectin 5 isoform 3 precursor |
| NM_003830.4 | NP_003821.1 | sialic acid-binding Ig-like lectin 5 isoform 1 precursor |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
16189514 | GOA |
SIGLEC5 Protein Structure
V-set: Immunoglobulin V-set domain (25 - 138)
ig: Immunoglobulin domain (160 - 214)
Ig_2: Immunoglobulin domain (257 - 318)
Ig_2: Immunoglobulin domain (349 - 389)
- 0
- 100
- 200
- 300
- 400
- 500
- 551 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
sialic acid-binding Ig-like lectin 5 |
|
SIGLEC5 Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
SIGLEC5 | O15389 | SLC7A8 | Homo sapiens | Q9UHI5 | 32296183 | |
|
Intra
|
SIGLEC5 | O15389 | SLC7A8 | Homo sapiens | Q9UHI5 | 32296183 | |
|
Intra
|
SIGLEC5 | O15389 | SLC7A8 | Homo sapiens | Q9UHI5 | 32296183 | |
|
Intra
|
SIGLEC5 | O15389 | VAC14 | Homo sapiens | Q08AM6 | 32296183 | |
|
Intra
|
SIGLEC5 | O15389 | VAC14 | Homo sapiens | Q08AM6 | 32296183 | |
|
Intra
|
SIGLEC5 | O15389 | VAC14 | Homo sapiens | Q08AM6 | 32296183 | |
|
Intra
|
SIGLEC5 | O15389 | TRIP13 | Homo sapiens | Q15645 | 16189514 | |
|
Intra
|
SIGLEC5 | O15389 | NAPB | Homo sapiens | Q9H115 | 32296183 | |
|
Intra
|
SIGLEC5 | O15389 | TLR4 | Homo sapiens | O00206 | 25187624 |
Recombinant SIGLEC5 Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P71023 | Siglec-5 Protein, Human (HEK293, His-Flag-Fc) | O15389 (E17-T434) | ≥ 95%, as determined by reducing SDS-PAGE. |
| HY-P72471 | Siglec-5 Protein, Human (HEK293, Fc) | O15389 (E17-T434) | ≥ 95%, as determined by reducing SDS-PAGE. |
| HY-P78203 | Siglec-5 Protein, Human (Biotinylated, HEK293, Fc) | O15389 (E17-T434) | ≥ 95%, as determined by Bis-Tris PAGE. |
| HY-P701038 | Siglec-5 Protein, Human (HEK293, His-Avi) | O15389 (E17-T434) | ≥ 95%, as determined by reducing SDS-PAGE. |
| HY-P701039 | Siglec-5 Protein, Human (Biotinylated, HEK293, His-Avi) | O15389 (E17-T434) | ≥ 95%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Periodontitis |
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| Gingival Disease |
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| Gastric Signet Ring Cell Adenocarcinoma |
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| Ovarian Cystic Teratoma |
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| Mature Teratoma Of The Ovary |
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| Ophthalmia Neonatorum |
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| Herpetic Whitlow |
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| Chorioretinal Scar |
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| Congenital Anomalies Of Kidney And Urinary Tract 2 |
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| Testicular Malignant Germ Cell Cancer |
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| Leukocyte Adhesion Deficiency, Type I |
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| Salpingitis |
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| Lemierre'S Syndrome |
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| Von Willebrand Disease, Type 1 |
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| Testicular Yolk Sac Tumor |
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| Subacute Bacterial Endocarditis |
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| Mixed Glioma |
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| Von Willebrand Disease, Type 3 |
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| Autoimmune Disease Of Exocrine System |
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| Developmental And Epileptic Encephalopathy 4 |
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| Neutrophilic Dermatosis, Acute Febrile |
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| Fallopian Tube Disease |
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| Potocki-Shaffer Syndrome |
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| Epiglottitis |
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| Congenital Disorder Of Glycosylation, Type Iib |
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| Von Willebrand Disease, Type 2 |
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| Suppurative Periapical Periodontitis |
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| Endocervical Carcinoma |
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| Angiodysplasia |
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| Sialuria |
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| Congenital Disorder Of Glycosylation, Type Iic |
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| Pseudo-Von Willebrand Disease |
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| Splenic Disease |
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| Factor Viii Deficiency |
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| Uterine Corpus Cancer |
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| Von Willebrand'S Disease |
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| Papillon-Lefevre Syndrome |
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| Autoimmune Polyendocrine Syndrome, Type Ii |
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| Endometrial Disease |
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| Coronavirus Infectious Disease |
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| Parasitic Protozoa Infectious Disease |
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| Chromophobe Renal Cell Carcinoma |
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| Chromosomal Deletion Syndrome |
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| Myopathy, Myofibrillar, 5 |
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| Marginal Zone B-Cell Lymphoma |
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| Primary Bacterial Infectious Disease |
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| Pyoderma Gangrenosum |
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| Autoimmune Disease Of Musculoskeletal System |
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| Endocervical Adenocarcinoma |
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| Disease By Infectious Agent |
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| Typhoid Fever |
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| Middle Ear Disease |
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| Endometritis |
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| Intestinal Schistosomiasis |
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| Visceral Leishmaniasis |
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| Severe Covid-19 |
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| Ocular Melanoma |
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| Aphthous Stomatitis |
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| Adrenal Cortical Hypofunction |
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| Salivary Gland Disease |
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| Mouth Disease |
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| Rectum Adenocarcinoma |
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| Blood Coagulation Disease |
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| Infective Endocarditis |
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| Ovarian Cystadenocarcinoma |
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| Endocardium Disease |
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| Immune System Disease |
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| Suppression Of Tumorigenicity 12 |
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| Bronchial Disease |
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| Parasitic Helminthiasis Infectious Disease |
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| Brain Glioma |
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| Ovarian Serous Cystadenocarcinoma |
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| Crohn'S Disease |
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| Pulmonary Disease, Chronic Obstructive |
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| Lymphoma, Mucosa-Associated Lymphoid Type |
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| Integumentary System Disease |
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| Bone Inflammation Disease |
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| Ovary Adenocarcinoma |
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| Respiratory System Disease |
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| Systemic Lupus Erythematosus |
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| Leukemia, Acute Myeloid |
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| Renal Cell Carcinoma, Nonpapillary |
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| Immune Deficiency Disease |
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| Connective Tissue Disease |
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| Skin Disease |
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| Nervous System Disease |
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| Body Mass Index Quantitative Trait Locus 11 |
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