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This gene encodes a soluble protein that binds alpha-trocopherol, a form of vitamin E, with high selectivity and affinity. This protein plays an important role in regulating vitamin E levels in the body by transporting vitamin E between membrane vesicles and facilitating the secretion of vitamin E from hepatocytes to circulating lipoproteins. Mutations in this gene cause hereditary vitamin E deficiency (ataxia with vitamin E deficiency, AVED) and retinitis pigmentosa.
alpha tocopherol transfer protein; alpha TTP; alpha-tocopherol transfer protein; alphaTTP; alpha-TTP; ATTP; AVED; tocopherol (alpha) transfer protein; tocopherol (alpha) transfer protein (ataxia (Friedreich-like) with vitamin E deficiency); Tocopherol transfer protein alpha; TPP1; TTP; TTP1; TTPA
100 µL
400 µL
100 µL
50 µg