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Mispem1Nsas
Endonuclease-mediated Allele Detail
Summary
Symbol: Mispem1Nsas
Name: mitotic spindle positioning; endonuclease-mediated mutation 1, Nobuya Sasaki
MGI ID: MGI:7486552
Synonyms: Misp KO
Gene: Misp  Location: Chr10:79656853-79666286 bp, + strand  Genetic Position: Chr10, 39.72 cM, cytoband C1
Alliance: Mispem1Nsas page
Mutation
origin
Strain of Origin:  FVB/NJcl
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/Cas9 genome editing technology was used to generate a 5-base deletion (TGCAC) in exon 2 of the gene. This deletion leads to a frame-shift and a premature stop codon (p.S220Qfs*2). Western blot analysis confirmed the absence of protein expression in the colon of homozygous mutant mice. (J:333842)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Misp Mutation:  20 strains or lines available
References
Original:  J:333842 Hiura K, et al., Mitotic spindle positioning protein (MISP) deficiency exacerbates dextran sulfate sodium (DSS)-induced colitis in mice. J Vet Med Sci. 2023 Feb 1;85(2):167-174
All:  1 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory