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Satb2em1Wanh
Endonuclease-mediated Allele Detail
Summary
Symbol: Satb2em1Wanh
Name: special AT-rich sequence binding protein 2; endonuclease-mediated mutation 1, Huijun Wang
MGI ID: MGI:7538988
Gene: Satb2  Location: Chr1:56833140-57017809 bp, - strand  Genetic Position: Chr1, 28.72 cM
Alliance: Satb2em1Wanh page
Mutation
origin
Strain of Origin:  Not Specified
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/cas9 mediated recombination using guide RNAs created an approximately 28 Kb deletion spanning exons 7 and 8. (J:333949)
Expression
In Mice Carrying this Mutation: 1 RNA-Seq or microarray experiment(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 Satb2 Mutation:  46 strains or lines available
References
Original:  J:333949 Guo Q, et al., In the developing cerebral cortex: axonogenesis, synapse formation, and synaptic plasticity are regulated by SATB2 target genes. Pediatr Res. 2022 Aug 26;
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
01/20/2026
MGI 6.24
The Jackson Laboratory