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Kcnj13em1Fvs
Endonuclease-mediated Allele Detail
Summary
Symbol: Kcnj13em1Fvs
Name: potassium inwardly-rectifying channel, subfamily J, member 13; endonuclease-mediated mutation 1, Francisco V Sepulveda
MGI ID: MGI:8348359
Synonyms: Kir7.1fl
Gene: Kcnj13  Location: Chr1:87314085-87322451 bp, - strand  Genetic Position: Chr1, 44.3 cM
Alliance: Kcnj13em1Fvs page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Endonuclease-mediated (Conditional ready)
Mutation:    Insertion
 
Mutation detailsIn two separate steps a loxP site was inserted into intron 1 and a second loxP site into intron 2 using sgRNAs and ssODN templates with CRISPR/Cas9 technology, creating a conditional-ready allele with exon 2 floxed. (J:386568)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
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 Kcnj13 Mutation:  24 strains or lines available
References
Original:  J:386568 Henao JC, et al., Role of the Choroid Plexus Kir7.1 Channel in the Regulation of Mouse Cerebrospinal Fluid K(+) Concentration. Acta Physiol (Oxf). 2025 Dec;241(12):e70129
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
05/26/2026
MGI 6.24
The Jackson Laboratory