|Bos taurus Gene: ASPM|
|Last Modified||2014-10-13 [Report errors or provide feedback]|
|Gene Name||abnormal spindle-like microcephaly-associated protein homolog|
asp (abnormal spindle) homolog, microcephaly associated (Drosophila)
|Useful resources||Stemformatics EHFPI ImmGen|
This gene does not have any Entrez summary - the following is the summary from its human ortholog ENSG00000066279:
This gene is the human ortholog of the Drosophila melanogaster 'abnormal spindle' gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts. Studies in mouse also suggest a role of this gene in mitotic spindle regulation, with a preferential role in regulating neurogenesis. Mutations in this gene are associated with microcephaly primary type 5. Multiple transcript variants encoding different isoforms have been found for this gene.[provided by RefSeq, May 2011]
|Genomic Location||Chromosome 16:77923530-77988157|
|Number of Interactions||
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
They are also associated with 10 interaction(s) predicted by orthology.
|UniProt Splice Variant|
|RNA Seq Atlas|