PLEK (Pleckstrin) is a Protein Coding gene. Diseases associated with PLEK include scott syndrome and amyotrophic lateral sclerosis type 2. Among its related pathways are Hemostasis and Response to elevated platelet cytosolic Ca2+. GO annotations related to this gene include protein homodimerization activity and phosphatidylinositol-3,4-bisphosphate binding. An important paralog of this gene is PLEK2.
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