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ASPM (gene)

ASPM
Identifiers
Aliases ASPM, ASP, Calmbp1, MCPH5, abnormal spindle microtubule assembly
External IDs OMIM: 605481 MGI: 1334448 HomoloGene: 7650 GeneCards: ASPM
Orthologs
Species Human Mouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_018136
NM_001206846

NM_009791

RefSeq (protein)

NP_001193775
NP_060606

NP_033921.3
NP_033921

Location (UCSC) Chr 1: 197.08 – 197.15 Mb Chr 1: 139.45 – 139.49 Mb
PubMed search

NM_018136
NM_001206846

NM_009791

NP_001193775
NP_060606

NP_033921.3
NP_033921

Abnormal spindle-like microcephaly-associated protein also known as abnormal spindle protein homolog or Asp homolog is a protein that in humans is encoded by the ASPM gene. ASPM is located on chromosome 1, band q31 (1q31). Defective forms of the ASPM gene are associated with autosomal recessive primary microcephaly.

"ASPM" is an acronym for "Abnormal Spindle-like, Microcephaly-associated", which reflects its being an ortholog to the Drosophila melanogaster "abnormal spindle" (asp) gene. The expressed protein product of the asp gene is essential for normal mitotic spindle function in embryonic neuroblasts and regulation of neurogenesis.


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