ALMS1 Polyclonal Antibody, 100ul Drug Development and Evaluation at least composed of ATXN7

at least composed of ATXN7

The enzyme plays an essential role in the carbohydrate metabolism

Members of this family have identical structural organization that consists of an N-terminal coiled-coil motif| a central Sec7 domain| and a C-terminal pleckstrin homology (PH) domain

This gene is a member of the WNT gene family

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ALMS1 Polyclonal Antibody, 100ul Drug Development and Evaluation at least composed of ATXN7ALMS1 encodes a protein containing a large tandem repeat domain as well as additional low complexity regions. The encoded protein (ALMS1, centrosome and basal body associated protein) functions in microtubule organization, particularly in the formation and maintanance of cilia. Mutations ALMS1 cause Alstrom syndrome. There is a pseudogene for ALMS1 located adjacent in the same region of chromosome 2. Alternative splice variants have been described but