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This gene belongs to the FAM161 family. It is expressed mainly in the retina. Mouse studies suggested that this gene is involved in development of retinal progenitors during embryogenesis, and that its activity is restricted to mature photoreceptors after birth. Mutations in this gene cause autosomal recessive retinitis pigmentosa-28. Alternatively spliced transcript variants have been identified.
4930430E16Rik; FAM161 centrosomal protein A; FAM161A; FAM161A, centrosomal protein; FAM161Afl; FAM161Ash; family with sequence similarity 161 member A; family with sequence similarity 161, member A; protein FAM161A; Protein FAM161A-like protein; retinitis pigmentosa 28 (autosomal recessive); RGD1304999; RP28
100 µg
100 µL
100 µL
100 µL
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