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KitlSl-42R
Chemically induced Allele Detail
Summary
Symbol: KitlSl-42R
Name: kit ligand; steel 42 Oak Ridge
MGI ID: MGI:2445946
Gene: Kitl  Location: Chr10:99851492-99936278 bp, + strand  Genetic Position: Chr10, 51.4 cM
Alliance: KitlSl-42R page
Mutation
origin
Strain of Origin:  101/Rl
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsNucleotide sequencing of Taq-generated RT-PCR products showed that this allele comprises a T-to-C transition. This eliminates exon 4 splice donor site G-GT by changing it to G-GA and produces an mRNA splicing defect through the use of a cryptic splice donor 8 bp downstream. There is little or no expression of wild-type mRNA. (J:80496)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 2 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 Kitl Mutation:  94 strains or lines available
References
Original:  J:80496 Rajaraman S, et al., An allelic series of mutations in the kit ligand gene of mice. I. Identification of point mutations in seven ethylnitrosourea-induced Kitl(Steel) alleles. Genetics. 2002 Sep;162(1):331-40
All:  3 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
11/12/2024
MGI 6.24
The Jackson Laboratory