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KitlSl-18H
Radiation induced Allele Detail
Nomenclature
Symbol: KitlSl-18H
Name: kit ligand; steel 18 Harwell
MGI ID: MGI:1856366
Gene: Kitl  Location: Chr10:100015630-100100416 bp, + strand  Genetic Position: Chr10, 51.4 cM
Mutation
origin
Strain of Origin:  (C3H/HeH x 101/H)F1
Mutation
description
Allele Type:    Radiation induced
Mutation:    Deletion
  KitlSl-18H involves 1 genes/genome features (Kitl) View all
 
Mutation detailsThis allele comprises a deletion that is cytologically apparent, removing ~2.5% of Chr 10. Southern blot analysis and pulsed field gel electrophoresis showed that this deletion is greater than 810kb. (J:3564, J:10748, J:31566)
Inheritance:    Semidominant
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Expression
In Structures Affected by this Mutation: 6 anatomical structures
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 1 strain available      Cell Lines: 0 lines available
Carrying any Kitl Mutation:  50 strains or lines available
References
Original:  J:18280 Cattanach BM, et al., A new steel allele with early post-implantation homozygous lethality. Mouse News Lett. 1988;80:157-58
All:  5 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
04/06/2021
MGI 6.16
The Jackson Laboratory