ASPM Products

Description

The ASPM gene is the human ortholog of the Drosophila melanogaster 'abnormal spindle' gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts (Bond et al., 2002). The mouse gene Aspm is expressed specifically in the primary sites of prenatal cerebral cortical neurogenesis.[supplied by OMIM]

Bioinformatics

Entrez	259266 Human
Uniprot	Q8IZT6 Human
Product By Gene ID	259266
Alternate Names	asp (abnormal spindle) homolog, microcephaly associated (Drosophila) Asp homolog ASP Calmbp1 FLJ43117 MCPH5DKFZp686N06184 microcephaly associated (Drosophila) microcephaly, primary autosomal recessive 5

Diseases related to ASPM

Discover more about diseases related to ASPM.

Microcephaly
Primary Microcephaly
Malignant Neoplasms
Neoplasms
Malignant Paraganglionic Neoplasm
Glioblastoma
Dwarfism
Severe Mental Retardation
Brain Neoplasms
Developmental Disabilities
Medulloblastoma
Congenital Abnormality
Liver Carcinoma
Mental Disorders
Cytogenetic Abnormality
Polymicrogyria
Malignant Neoplasm Of Breast

Pathways for ASPM

View related products by pathway and learn more about each of the pathways below.

Mitosis
Neurogenesis
Brain Development
Cell Cycle
Cell Division
Cytokinesis
Cell Proliferation
Cognition
Localization
Pathogenesis
Chromosome Segregation
Stem Cell Proliferation
Cell Death
Mitotic Cell Cycle
Immune Response
Hypersensitivity
Spindle Assembly
Dna Repair
Cell Adhesion
Cell Cycle Checkpoint

PTMs for ASPM

Learn more about PTMs related to ASPM.

Methylation
Demethylation
Phosphorylation
Cleavage
Acetylation

Bioinformatics Tool for ASPM

Discover related pathways, diseases and genes to ASPM. Need help? Read the Bioinformatics Tool Guide for instructions on using this tool.