A synthesized peptide derived from human VIPR2, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human VIP Receptor 1, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human Virion infectivity factor, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human VISA, corresponding to a region within C-terminal amino acids.
VSIR (V-Set Immunoregulatory Receptor, also known as VISTA) is a Protein Coding gene. VISTA is an immunoregulatory receptor that inhibits the T-cell response. It may promote differentiation of embryonic stem cells, by inhibiting BMP4 signaling. VSIR, or V-set immunoregulatory receptor, could be involved in the pathogenesis of chronic rhinosinusitis with nasal polyps. V-domain Immunoglobulin Suppressor of T cell Activation (VISTA) is an inhibitory immune-checkpoint molecule that suppresses CD4+ and CD8+ T cell activation when expressed on antigen-presenting cells. VSIR is broadly expressed in the spleen, bone marrow, and other tissues. Diseases associated with VSIR include Ichthyosis, Congenital, Autosomal Recessive 6, and Monckeberg Arteriosclerosis. An important paralog of this gene is VSIG8.
A synthesized peptide derived from human Vitamin D Binding protein, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human Vitamin D Receptor, corresponding to a region within the internal amino acids.
A synthetic peptide from human Vitamin D Receptor
A synthesized peptide derived from Human VKORC1L1.
A synthesized peptide derived from human VLDL Receptor, corresponding to a region within N-terminal amino acids.
The low density lipoprotein receptor (LDLR) gene family consists of cell surface proteins involved in receptor-mediated endocytosis of specific ligands. This gene encodes a lipoprotein receptor that is a member of the LDLR family and plays important roles in VLDL-triglyceride metabolism and the reelin signaling pathway. Mutations in this gene cause VLDLR-associated cerebellar hypoplasia. Alternative splicing generates multiple transcript variants encoding distinct isoforms for this gene.
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