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Disease Info Card
Griscelli Syndrome, Type 2
Information about Griscelli Syndrome, Type 2: characteristics, related genes and pathways, plus antibodies you can use for research. This page is being enriched constantly, if you see some information you would like this page to include please send your suggestions to us.
Overview of Griscelli Syndrome, Type 2
Most recent studies have shown that Griscelli Syndrome, Type 2 shares some biological mechanisms with albinism, chediak-higashi-syndrome, demyelinating-diseases, epstein-barr-virus-infections, familial-hemophagocytic-lymphocytosis, histiocytosis-haematophagic, hypopigmentation-disorder, hypopigmentation-immunodeficiency-disease, immune-system-diseases, immunologic-deficiency-syndromes, infective-disorder, lymphohistiocytosis-hemophagocytic, lymphoproliferative-disorders, malignant-neoplasms, piebaldism, primary-immune-deficiency-disorder, sequelae-aspects.
Among the many pathways, these few ones have gauged particular interests from scientists studying Griscelli Syndrome, Type 2, and have been seen in publications frequently: Antibody-dependent Cellular Cytotoxicity, Coagulation, Conjugation, Cytokine Production, Exocytosis, Hypersensitivity, Immune Response, Insulin Secretion, Localization, Lymphocyte Homeostasis, Macrophage Activation, Melanosome Transport, Pigmentation, Protein Folding, Secretion, Transport
Quite a number of genes have been found to play important roles in Griscelli Syndrome, Type 2, such as ELANE, FCGR3B, FHL2, FHL3, HAX1, LAMP1, LYST, MLPH, MYO5A, PNPLA4, RAB27A, SH2D1A, UNC13D, XIAP. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.
In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.