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KitlSl-29H
Spontaneous Allele Detail
Summary
Symbol: KitlSl-29H
Name: kit ligand; steel 29 Harwell
MGI ID: MGI:5314350
Gene: Kitl  Location: Chr10:99851492-99936278 bp, + strand  Genetic Position: Chr10, 51.4 cM
Alliance: KitlSl-29H page
Mutation
origin
Strain of Origin:  (C3H/HeH x 101/H)F1
Mutation
description
Allele Type:    Spontaneous
Inheritance:    Dominant
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
Notes
Most likely to be a spontaneous mutation. Steel phenotype first seen in 19 out of 90 offspring from a female that looked wild-type for steel, but had a (heritable) head-bobbing phenotype. This female (probably a mosaic for Sl-29H) was the offspring of a male that received TEM + HU + HU +6Gy x-rays.
References
Original:  J:169366 MouseBookTM, Information obtained from MouseBookTM, Medical Research Council Mammalian Genetics Unit, Harwell, UK. Unpublished. 2005-2013;
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
12/10/2024
MGI 6.24
The Jackson Laboratory