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Qkitm1Imeg
Targeted Allele Detail
Summary
Symbol: Qkitm1Imeg
Name: quaking, KH domain containing RNA binding; targeted mutation 1, Institute of Molecular Embryology and Genetics
MGI ID: MGI:3033861
Synonyms: qkI-
Gene: Qki  Location: Chr17:10425480-10538706 bp, - strand  Genetic Position: Chr17, 7.75 cM
Alliance: Qkitm1Imeg page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:88215
Parent Cell Line:  E14.1 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout, Reporter)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsPart of intron 1 and the first part of the coding sequence in exon 2, which includes the initiation sequence and the codons for the first 44 amino acids, were replaced with an IRES and a betageo fusion gene. This removes the highly conserved QUA1 domain in the encoded protein. Absence of transcription of the endogenous gene was demonstrated by RT-PCR. Beta-galactosidase is expressed from this allele. (J:88215)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 7 anatomical structure(s)
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Qki Mutation:  28 strains or lines available
References
Original:  J:88215 Li Z, et al., Defective smooth muscle development in qkI-deficient mice. Dev Growth Differ. 2003 Oct-Dec;45(5-6):449-62
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
10/29/2024
MGI 6.24
The Jackson Laboratory