Aladin Polyclonal Antibody, 50ul Cellular Function Assays The gene is expressed in

The gene is expressed in male germ cells

Substrates of the encoded protein include the transcription factor ATF2 and the microtubule dynamics regulator stathmin

The gene is located near the Smith-Magenis syndrome region on chromosome 17

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Aladin Polyclonal Antibody, 50ul Cellular Function Assays The gene is expressed inAladin encoded by AAAS is a member of the WD repeat family of regulatory proteins and may be involved in normal development of the peripheral and central nervous system. The encoded protein is part of the nuclear pore complex and is anchored there by NDC1. Defects in this gene are a cause of achalasia addisonianism alacrima syndrome (AAAS), also called triple A syndrome or Allgrove syndrome. Two transcript variants encoding different isoforms have