|Institutional Source||Beutler Lab|
|Gene Name||abnormal spindle microtubule assembly|
|Synonyms||Aspm, Sha1, MCPH5, D330028K02Rik, Calmbp1|
|Is this an essential gene?||Non essential (E-score: 0.000)|
|Stock #||R7237 (G1)|
|Chromosomal Location||139454772-139494091 bp(+) (GRCm38)|
|Type of Mutation||missense|
|DNA Base Change (assembly)||T to A at 139477929 bp (GRCm38)|
|Amino Acid Change||Methionine to Lysine at position 1518 (M1518K)|
|Ref Sequence||ENSEMBL: ENSMUSP00000059159 (fasta)|
|Gene Model||predicted gene model for transcript(s): [ENSMUST00000053364] [ENSMUST00000200083]|
|AlphaFold||no structure available at present|
AA Change: M1518K
PolyPhen 2 Score 0.814 (Sensitivity: 0.84; Specificity: 0.93)
AA Change: M1518K
|Coding Region Coverage||
|Validation Efficiency||98% (83/85)|
FUNCTION: [Summary is not available for the mouse gene. This summary is for the human ortholog.] 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]
PHENOTYPE: Mice homozygous for protein-truncating gene trap mutations of this gene exhibit decreased body weight, microcephaly, a severe reduction in brain, testis and ovary weight, oligozoospermia and asthenospermia, and reduced fertility in both sexes. [provided by MGI curators]
|Allele List at MGI|
|Other mutations in this stock||
|Other mutations in Aspm||
(F):5'- TTGTCATCCAGAGAAGAGTTCGG -3'
(R):5'- CTCCTGGCTGAAATGGAAGC -3'
(F):5'- ATCCAGAGAAGAGTTCGGTGCTTTC -3'
(R):5'- GCTCGGAAATGAGTCTGAATTG -3'