CD1B - CD1b molecule Gene
Also Known as R1; CD1; CD1A
Species: Homo sapiens
About CD1B
This gene has 2 transcripts (splice variants), 459 orthologues and 22 paralogues. Low expression observed in reference dataset.
Summary
This gene encodes a member of the CD1 family of transmembrane glycoproteins, which are structurally related to the major histocompatibility complex (MHC) proteins and form heterodimers with beta-2-microglobulin. The CD1 proteins mediate the presentation of primarily lipid and glycolipid antigens of self or microbial origin to T cells. The human genome contains five CD1 family genes organized in a cluster on chromosome 1. The CD1 family members are thought to differ in their cellular localization and specificity for particular lipid ligands. The protein encoded by this gene localizes to late endosomes and lysosomes via a tyrosine-based motif in the cytoplasmic tail, and requires vesicular acidification to bind lipid antigens. [provided by RefSeq, Jul 2008]
CD1B Products (1)
| mRNA | Protein | Name |
|---|---|---|
| NM_001764.3 | NP_001755.1 | T-cell surface glycoprotein CD1b precursor |
| Molecular Function GO Annotation | Evidence | References | Source |
|---|---|---|---|
| enables protein binding |
IPI
IPI: Inferred from physical interaction
|
12118248 | GOA |
CD1B Protein Structure
C1-set: Immunoglobulin C1-set domain (220 - 287)
- 0
- 100
- 200
- 300
- 333 a.a.
| Protein Preferred Names | Protein Names | |
|---|---|---|
|
T-cell surface glycoprotein CD1b |
|
CD1B Protein-protein interaction Information
|
Type
|
Protein Name | Protein ID | Interactor | Interactor Species | Interactor ID | Detection Method | References |
|---|---|---|---|---|---|---|---|
|
Intra
|
CD1B | P29016 | B2M | Homo sapiens | P61769 | 14764708 | |
|
Intra
|
CD1B | P29016 | B2M | Homo sapiens | P61769 | 33961781 | |
|
Intra
|
CD1B | P29016 | B2M | Homo sapiens | P61769 | 28514442 |
Recombinant CD1B Proteins
| Cat. No. | Product Name | Accession | Purity |
|---|---|---|---|
| HY-P75438 | CD1B Protein, Human (HEK293, Fc) | P29016 (S18-S303) | ≥ 95%, as determined by reducing SDS-PAGE. |
Related Diseases
| Diseases | Alias | |
|---|---|---|
| Follicular Dendritic Cell Sarcoma |
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| Non-Langerhans-Cell Histiocytosis |
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| Interdigitating Dendritic Cell Sarcoma |
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| Adult Xanthogranuloma |
|
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| Rhinoscleroma |
|
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| Langerhans Cell Sarcoma |
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| Histiocytic And Dendritic Cell Cancer |
|
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| Reticulohistiocytic Granuloma |
|
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| Juvenile Xanthogranuloma |
|
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| Multicentric Reticulohistiocytosis |
|
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| Mycobacterium Tuberculosis 1 |
|
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| Orbital Cancer |
|
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| Erdheim-Chester Disease |
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| Granuloma Annulare |
|
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| Fibrosarcoma Of Bone |
|
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| Cobblestone Retinal Degeneration |
|
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| Langerhans Cell Histiocytosis |
|
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| Granulomatous Dermatitis |
|
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| Tuberculoid Leprosy |
|
|
| Histiocytosis-Lymphadenopathy Plus Syndrome |
|
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| Spongiotic Dermatitis |
|
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| Polyclonal Hypergammaglobulinemia |
|
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| Mycosis Fungoides |
|
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| Mixed Type Thymoma |
|
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| Malignant Histiocytic Disease |
|
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| Exophthalmos |
|
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| Lymphoid Interstitial Pneumonia |
|
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| Orbital Disease |
|
|
| Mixed Phenotype Acute Leukemia, T/Myeloid |
|
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| Necrobiosis Lipoidica |
|
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| Seborrheic Dermatitis |
|
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| Histiocytic Sarcoma |
|
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| Central Diabetes Insipidus |
|
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| Lichen Nitidus |
|
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| Kimura Disease |
|
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| Dendritic Cell Thymoma |
|
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| Otorrhea |
|
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| Epithelial Malignant Thymoma |
|
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| Large Cell Acanthoma |
|
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| Interstitial Pneumonitis, Desquamative, Familial |
|
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| Keratosis, Seborrheic |
|
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| Frontal Sinus Benign Neoplasm |
|
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| Lichen Disease |
|
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| Chronic Laryngitis |
|
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| Cortical Thymoma |
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| Connective Tissue Benign Neoplasm |
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| Geographic Tongue |
|
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| Lepromatous Leprosy |
|
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| Beach Ear |
|
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| Acanthoma |
|
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| Mite Infestation |
|
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| Folliculitis |
|
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| Leprosy 3 |
|
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| Balloon Cell Malignant Melanoma |
|
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| Vulvar Proximal-Type Epithelioid Sarcoma |
|
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| Central Epithelioid Sarcoma |
|
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| Diencephalic Astrocytoma |
|
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| T-Cell Prolymphocytic Leukemia |
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| Hypersensitivity Reaction Type Iv Disease |
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| Thymus Gland Disease |
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| Thymus Cancer |
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| Nodular Tenosynovitis |
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| Skin Disease |
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| Meningioma, Familial |
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