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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Tg(PGK1-KITLG*220)441Daw
transgene insertion 441, David A Williams
MGI:3817558
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
cx1
KitlSl/Kitl+
Tg(PGK1-KITLG*220)441Daw/0
involves: C3H MGI:3817636
cx2
KitW/Kit+
Tg(PGK1-KITLG*220)441Daw/0
involves: C3H/HeJ MGI:3817635
tg3
Tg(PGK1-KITLG*220)441Daw/Tg(PGK1-KITLG*220)441Daw C3H/HeJ-Tg(PGK1-KITLG*220)441Daw MGI:3817633


Genotype
MGI:3817636
cx1
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 (94 available)
Tg(PGK1-KITLG*220)441Daw mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• 18% of offspring show more severe pigment loss than either parental strain

hematopoietic system
• numbers of connective tissue mast cells are greatly reduced relative to controls

immune system
• numbers of connective tissue mast cells are greatly reduced relative to controls

integument
• 18% of offspring show more severe pigment loss than either parental strain




Genotype
MGI:3817635
cx2
Allelic
Composition
KitW/Kit+
Tg(PGK1-KITLG*220)441Daw/0
Genetic
Background
involves: C3H/HeJ
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
KitW mutation (10 available); any Kit mutation (182 available)
Tg(PGK1-KITLG*220)441Daw mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• 46% of mice show coat color similar to hemizygous transgenics or heterozygous KitW animals, while 29% show wild-type agouti coat coloring
• 25% of double mutants have a more severe deficiency in coat color pigmentation with large areas of hypopigmentation

hematopoietic system
• numbers of connective tissue mast cells are greatly reduced relative to controls

immune system
• numbers of connective tissue mast cells are greatly reduced relative to controls

integument
• 46% of mice show coat color similar to hemizygous transgenics or heterozygous KitW animals, while 29% show wild-type agouti coat coloring
• 25% of double mutants have a more severe deficiency in coat color pigmentation with large areas of hypopigmentation




Genotype
MGI:3817633
tg3
Allelic
Composition
Tg(PGK1-KITLG*220)441Daw/Tg(PGK1-KITLG*220)441Daw
Genetic
Background
C3H/HeJ-Tg(PGK1-KITLG*220)441Daw
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Tg(PGK1-KITLG*220)441Daw mutation (1 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
pigmentation
• mice have prominent white head blaze (diamond-shaped white spot)
• belly spot is larger than in heterozygous mice
• mice show secondary spotting over cervical region and occasionally elsewhere

hematopoietic system
• development is abnormal in homozygotes

immune system
• development is abnormal in homozygotes

integument
• mice have prominent white head blaze (diamond-shaped white spot)
• belly spot is larger than in heterozygous mice
• mice show secondary spotting over cervical region and occasionally elsewhere

endocrine/exocrine glands
• development is abnormal in homozygotes





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last database update
12/10/2024
MGI 6.24
The Jackson Laboratory