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Slc26a9em1(cre)Sms
Endonuclease-mediated Allele Detail
Summary
Symbol: Slc26a9em1(cre)Sms
Name: solute carrier family 26, member 9; endonuclease-mediated mutation 1, Suzanne L Mansour
MGI ID: MGI:6715244
Synonyms: Slc26a9P2ACre
Gene: Slc26a9  Location: Chr1:131671760-131699242 bp, + strand  Genetic Position: Chr1, 57.18 cM
Alliance: Slc26a9em1(cre)Sms page
Mutation
origin
Strain of Origin:  C57BL/6
Mutation
description
Allele Type:    Endonuclease-mediated (Recombinase)
Mutations:    Insertion, Single point mutation
 
Slc26a9em1(cre)Sms expression driven by 1 gene
 
Mutation detailsCRISPR-targeting inserted a P2A sequence and rec recombinase gene down stream of the coding sequence altering the stop codon. (J:290227)
Recombinase
activity
Activity:
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Driver: Slc26a9 (mouse)
Summary of all recombinase alleles driven by Slc26a9.
 

Expression
In Mice Carrying this Mutation: 15 assay results
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 Slc26a9 Mutation:  76 strains or lines available
References
Original:  J:290227 Urness LD, et al., Slc26a9(P2ACre) : a new CRE driver to regulate gene expression in the otic placode lineage and other FGFR2b-dependent epithelia. Development. 2020 Jul 8;147(13):dev191015
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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Funding Information
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last database update
06/12/2024
MGI 6.13
The Jackson Laboratory