CLEC1B | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | CLEC1B , 1810061I13Rik, CLEC2, CLEC2B, PRO1384, QDED721, C-type lectin domain family 1 member B | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 606783 MGI: 1913287 HomoloGene: 49468 GeneCards: CLEC1B | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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C-type lectin domain family 1 member B is a protein that in humans is encoded by the CLEC1B gene. [5] [6] [7]
Natural killer (NK) cells express multiple calcium-dependent (C-type) lectin-like receptors, such as CD94 (KLRD1; MIM 602894) and NKG2D (KLRC4; MIM 602893), that interact with major histocompatibility complex class I molecules and either inhibit or activate cytotoxicity and cytokine secretion. CLEC2 is a C-type lectin-like receptor expressed in myeloid cells and NK cells.[supplied by OMIM] [7]
CD94, also known as killer cell lectin-like receptor subfamily D, member 1 (KLRD1) is a human gene.
Oxidized low-density lipoprotein receptor 1 also known as lectin-type oxidized LDL receptor 1 (LOX-1) is a protein that in humans is encoded by the OLR1 gene.
CD69 is a human transmembrane C-Type lectin protein encoded by the CD69 gene. It is an early activation marker that is expressed in hematopoietic stem cells, T cells, and many other cell types in the immune system. It is also implicated in T cell differentiation as well as lymphocyte retention in lymphoid organs.
TYRO protein tyrosine kinase-binding protein is an adapter protein that in humans is encoded by the TYROBP gene.
C-C chemokine receptor type 11 is a protein that in humans is encoded by the CCRL1 gene.
CD244 also known as 2B4 or SLAMF4 is a protein that in humans is encoded by the CD244 gene.
CD93 is a protein that in humans is encoded by the CD93 gene. CD93 is a C-type lectin transmembrane receptor which plays a role not only in cell–cell adhesion processes but also in host defense.
C-type lectin domain family 7 member A or Dectin-1 is a protein that in humans is encoded by the CLEC7A gene. CLEC7A is a member of the C-type lectin/C-type lectin-like domain (CTL/CTLD) superfamily. The encoded glycoprotein is a small type II membrane receptor with an extracellular C-type lectin-like domain fold and a cytoplasmic domain with a partial immunoreceptor tyrosine-based activation motif. It functions as a pattern-recognition receptor for a variety of β-1,3-linked and β-1,6-linked glucans from fungi and plants, and in this way plays a role in innate immune response. Expression is found on myeloid dendritic cells, monocytes, macrophages and B cells. Alternate transcriptional splice variants, encoding different isoforms, have been characterized. This gene is closely linked to other CTL/CTLD superfamily members on chromosome 12p13 in the natural killer gene complex region.
NKG2-F type II integral membrane protein is a protein that in humans is encoded by the KLRC4 gene.
CD226, PTA1 or DNAM-1 is a ~65 kDa immunoglobulin-like transmembrane glycoprotein expressed on the surface of natural killer cells, NK T cell, B cells, dendritic cells, hematopoietic precursor cells, platelets, monocytes and T cells.
Killer cell lectin-like receptor subfamily B, member 1, also known as KLRB1, NKR-P1A or CD161, is a human gene.
SLAM family member 6 is a protein that in humans is encoded by the SLAMF6 gene.
Interleukin 21 receptor is a type I cytokine receptor. IL21R is its human gene.
Hematopoietic cell signal transducer is a protein that in humans is encoded by the HCST gene.
Endosialin is a protein that in humans is encoded by the CD248 gene.
C-type lectin domain family 2 member D is a protein that in humans is encoded by the CLEC2D gene.
C-type lectin domain family 4 member A is a protein that in humans is encoded by the CLEC4A gene.
C-type lectin domain family 1 member A is a protein that in humans is encoded by the CLEC1A gene.
C-type lectin domain family 2 member B is a protein that in humans is encoded by the CLEC2B gene.
C-type lectin domain family 12 member A is a protein that in humans is encoded by the CLEC12A gene.