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Phenotypes Associated with This Genotype
Genotype
MGI:3817636
Allelic
Composition		 KitlSl/Kitl+
Tg(PGK1-KITLG*220)441Daw/0
Genetic
Background		 involves: C3H
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
KitlSl mutation (3 available); any Kitl mutation (92 available)
Tg(PGK1-KITLG*220)441Daw mutation (1 available)
♀ phenotype observed in females
♂ phenotype observed in males
N normal phenotype
pigmentation
abnormal coat/hair pigmentation ( J:32600 )
• 18% of offspring show more severe pigment loss than either parental strain

hematopoietic system
decreased mast cell number ( J:32600 )
• numbers of connective tissue mast cells are greatly reduced relative to controls

immune system
decreased mast cell number ( J:32600 )
• numbers of connective tissue mast cells are greatly reduced relative to controls

integument
abnormal coat/hair pigmentation ( J:32600 )
• 18% of offspring show more severe pigment loss than either parental strain

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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Send questions and comments to User Support. 		last database update
03/25/2025
MGI 6.24 		The Jackson Laboratory