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Protein Domain : Abnormal spindle-like microcephaly-associated protein

Primary Identifier  IPR029955 Type  Family
Short Name  ASPM
description  Abnormal spindle-like microcephaly-associated protein (ASPM) is a mitotic spindle protein. In Drosophila it is known as Asp, and it is required to maintain the structure of the centrosomal microtubule organising centre (MTOC) during mitosis []. In humans it is involved in spindle organisation, spindle orientation and cytokinesis []. Mutations in the ASPM gene cause autosomal recessive primary microcephaly (MCPH), which is a rare Mendelian disorder characterised by a congenital deficiency of foetal brain growth, particularly affecting the neocortex [].

0 Child Features

0 Parent Features

4 Protein Domain Regions