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Slc22a14em1Fjw
Endonuclease-mediated Allele Detail
Summary
Symbol: Slc22a14em1Fjw
Name: solute carrier family 22 (organic cation transporter), member 14; endonuclease-mediated mutation 1, Wataru Fujii
MGI ID: MGI:6356365
Synonyms: Slc22a14-, Slc22a14 KO
Gene: Slc22a14  Location: Chr9:118998523-119019473 bp, - strand  Genetic Position: Chr9, 71.33 cM
Alliance: Slc22a14em1Fjw page
Mutation
origin
Strain of Origin:  C57BL/6N
Mutation
description
Allele Type:    Endonuclease-mediated (Null/knockout)
Mutation:    Intragenic deletion
 
Mutation detailsCRISPR/Cas9 mutagenesis induced a deletion of exons 7-9, as confirmed by genomic DNA sequencing and genome PCR. RT-PCR and Western blot analysis revealed that expression of mRNA and its product were prominently reduced in homozygous mutant testes. (J:277914)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 1 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 Slc22a14 Mutation:  29 strains or lines available
References
Original:  J:277914 Maruyama SY, et al., A critical role of solute carrier 22a14 in sperm motility and male fertility in mice. Sci Rep. 2016 Nov 4;6:36468
All:  2 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
04/09/2024
MGI 6.23
The Jackson Laboratory