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Type Coisogenic; Mutant Strain; Spontaneous Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse Generation N6+p Description
KitlSl-20J is a dominant allele. On the C57BL/6J background heterozygotes have a light black coat color with lighter tail and feet and a steel colored belly with a belly spot. Heterozygotes of both sexes are viable and fertile.
Strains carrying other alleles of Kitl
000090 129S1/Sv-Oca2+ Tyr+ KitlSl-J/J 002993 B6.Cg-KitlSl-18H/EiJ 008656 B6.Cg-KitlSl-gb/MbeJ 000124 B6.Cg-KitlSl Krt71Ca/J 000160 B6.D2-KitlSl-d/J 000291 C3FeLe.Cg-a/a Hm KitlSl Krt71Ca-J/J 001380 C3Sn.Cg-KitlSl-con/J 000979 STOCK KitlSl-16J/J 000161 WB.D2-KitlSl-d/J 000693 WC/ReJ KitlSl/J 100401 WCB6F1/J KitlSl KitlSl-d View Strains carrying other alleles of Kitl (11 strains)
JAX® NOTES, February 2001; 481. Mgf Gene Name Changes to Kitl.
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
KitlSl-20J/Kitl+
C57BL/6J
- pigmentation phenotype
- belly spot (MGI Ref ID J:86436)
- heterozygous mice have either a white belly spot or dilute ventral pigmentation
- skin/coat/nails phenotype
- belly spot (MGI Ref ID J:86436)
- heterozygous mice have either a white belly spot or dilute ventral pigmentation
KitlSl-20J/KitlSl-20J
C57BL/6J
- lethality-prenatal/perinatal
- lethality throughout fetal growth and development (MGI Ref ID J:86436)
- no homozygous mice are born
- normal ratio of genotypes at E14.5
- growth/size phenotype
- decreased fetal size (MGI Ref ID J:86436)
- homozygous embryos were runted at E14.5
- hematopoietic system phenotype
- abnormal erythropoiesis (MGI Ref ID J:86436)
- reduced CFU-E/BFU-E ratio indicating reduced erythroid progenitors during terminal differentiation
- reproductive system phenotype
- absent primordial germ cells (MGI Ref ID J:86436)
- no primordial germ cells present at E13.5
- liver/biliary system phenotype
- pale liver (MGI Ref ID J:86436)
- skin/coat/nails phenotype
- pallor (MGI Ref ID J:86436)
- fetus pale at E14.5
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:KitlSl-20J related
Cancer Research
Growth Factors/Receptors/Cytokines
Increased Tumor Incidence
Gonadal Tumors: ovarian and testicular
Dermatology Research
Color and White Spotting Defects
Developmental Biology Research
Neural Crest Defects
Endocrine Deficiency Research
Bone/Bone Marrow Defects
Gonad Defects
Hypothalamus/Pituitary Defects
Skin Defects
Immunology and Inflammation Research
Growth Factors/Receptors/Cytokines
Immunodeficiency
Mast Cell Deficiency
Neurobiology Research
Vestibular and Hearing Defects
Reproductive Biology Research
Developmental Defects Affecting Gonads
germ cell deficient
Fertility Defects
Gonadal Tumors
ovarian and testicular
Research Tools
Immunology and Inflammation Research
Mast Cell Deficiency
Sensorineural Research
Vestibular and Hearing Defects
| Allele Symbol | KitlSl-20J | ||
|---|---|---|---|
| Allele Name | steel 20 Jackson | ||
| Allele Type | Spontaneous | ||
| Strain of Origin | C57BL/6J | ||
| Gene Symbol and Name | Kitl, kit ligand | ||
| Chromosome | 10 | ||
| Gene Common Name(s) | Clo; Con; DKFZp686F2250; FPH2; Gb; KL-1; MGF; Mgf; SCF; SF; SHEP7; SLF; Sl; Steel; Steel factor; cloud gray; contrasted; grizzle-belly; mast cell growth factor; steel; stem cell factor; | ||
| General Note |
This spontaneous mutation arose in a C57BL/6J breeding colony at The Jackson Laboratory. | ||
| Molecular Note | Long-range PCR demonstrated that this mutation is an in-frame tandem duplication of exon 3 which also involves duplication of introns 3 and 2. At the junction between intron 3 and intron 2 there is an inverted 141 bp duplication of a sequence found later in intron 2. The duplication of exon 3 results in a loss of function in the expressed protein due either to defective binding to its receptor or failure to activate the receptor once bound. [MGI Ref ID J:86436] | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Genotyping resources and troubleshooting
KitlSl-20J relatedChandra S; Kapur R; Chuzhanova N; Summey V; Prentice D; Barker J; Cooper DN; Williams DA. 2003. A rare complex DNA rearrangement in the murine Steel gene results in exon duplication and a lethal phenotype. Blood 102(10):3548-55. [PubMed: 12881302] [MGI Ref ID J:86436]
Currently there no information available for this strain. This may be due to the supply level of this strain.
| Pricing for USA, Canada and Mexico shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $1900.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Pricing for International shipping destinations |
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Animals Provided
Price (US dollars $) Cryorecovery Fee $2470.00 At least two mice that carry the mutation (if it is a mutant strain) will be provided. Their genotypes may not reflect those discussed in the strain description. Please inquire for possible genotypes and see additional details below.
| Standard Supply | Cryopreserved. Ready for recovery. Please refer to pricing and supply notes for further information. |
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| Supply Notes |
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Purchasing Information
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Contact Information
Orders & Technical Support
Tel: 1-800-422-6423 or 1-207-288-5845
Fax: 1-207-288-6150
Technical Support Email Form
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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