LC7L3 Polyclonal Antibody, 20ul Glassware Sets Mutations in this gene are

Mutations in this gene are found in patients diagnosed with Stargardt disease| a form of juvenile-onset macular degeneration

and may be involved in a range of nuclear processes including translational initiation

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in the maintenance of gut structure and function

possibly by locally regulating phosphorylation of microtubule-associated proteins

LC7L3 Polyclonal Antibody, 20ul Glassware Sets Mutations in this gene areThis gene encodes a protein with an N terminal half that contains cysteine histidine motifs and leucine zipper like repeats, and the C terminal half is rich in arginine and glutamate residues (RE domain) and arginine and serine residues (RS domain). This protein localizes with a speckled pattern in the nucleus, and could be involved in the formation of splicesome via the RE and RS domains. Two alternatively spliced transcript variants encoding the