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KitlSl-1Neu
Spontaneous Allele Detail
Summary
Symbol: KitlSl-1Neu
Name: kit ligand; steel 1 Neuherberg
MGI ID: MGI:2447294
Synonyms: MgfSl-1Neu, Sl-1Neu
Gene: Kitl  Location: Chr10:99851492-99936278 bp, + strand  Genetic Position: Chr10, 51.4 cM
Alliance: KitlSl-1Neu page
Mutation
origin
Strain of Origin:  (102/El x C3H/El)F1
Mutation
description
Allele Type:    Spontaneous
Mutation:    Single point mutation
 
Mutation detailsSequence analysis of mice homozygous for this allele showed an A-to-G transition in the start codon, changing it from methionine to valine (p.M1V). The loss of the start codon is predicted to result in an N-terminally truncated protein. (J:37172)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
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:37172 Graw J, et al., Molecular analysis of two new Steel mutations in mice shows a transversion or an insertion. Mamm Genome. 1996 Nov;7(11):843-6
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
11/12/2024
MGI 6.24
The Jackson Laboratory