Summary | Mutation origin | Mutation description | Expression | Phenotypes | Find Mice (IMSR) | References

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

Strain of Origin:

C3H/HeH

Allele Type:    Chemically induced (ENU) Mutation:    Single point mutation   Mutation details: Sequence 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

View phenotypes and curated references for all genotypes (concatenated display).

In Mice Carrying this Mutation:	18 assay results
In Structures Affected by this Mutation:	5 anatomical structure(s)

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:	92 strains or lines available

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)