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This locus encodes a protein that is likely secreted and may function in hematopoiesis. A mutation at this locus has been associated with amelogenesis imperfecta and gingival hyperplasia syndrome. Alternatively spliced transcript variants have been identified.
AI1G; AI606893; AIGFS; FAM20A; family with sequence similarity 20 member A; family with sequence similarity 20, member A; FP2747; ortholog of human family with sequence similarity 20, member A FAM20A; protein FAM20A; pseudokinase FAM20A; RGD1306364; UNQ9388/PRO34279
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