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KitlSl-17H
Chemically induced Allele Detail
Summary
Symbol: KitlSl-17H
Name: kit ligand; steel 17 Harwell
MGI ID: MGI:1857739
Synonyms: Steel17H
Gene: Kitl  Location: Chr10:99851492-99936278 bp, + strand  Genetic Position: Chr10, 51.4 cM
Alliance: KitlSl-17H page
Mutation
origin
Strain of Origin:  C3H/HeH
Mutation
description
Allele Type:    Chemically induced (ENU)
Mutation:    Single point mutation
 
Mutation detailsSequence analysis showed that this allele comprises a T-to-A transversion 11 bp upstream of exon 8 in intron 7. Sequencing of the complete coding region of the mRNA of this allele shows that this transversion results in the deletion of exon 8. (J:2880)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Mice Carrying this Mutation: 18 assay results
In Structures Affected by this Mutation: 5 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:24739 Peters J, A new steel allele which does not lead to dilution of coat colour. Mouse News Lett. 1987;77:125-6
All:  12 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
12/10/2024
MGI 6.24
The Jackson Laboratory