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Former Names MgfSl-con (Changed: 15-DEC-04 ) Type Congenic; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Additional information on Congenic nomenclature. Species laboratory mouse Background Strain C3H/HeSnJ Donor Strain (C3H/HeH x 101/H)F1 Generation N12p Description
Both homozygous and heterozygous mice with the contrasted induced mutation (KitlSl-con) are viable. Male homozygous mutant mice are fertile but females are usually sterile. Mice heterozygous for the contrasted mutation are recognizable soon after birth by dark pigmentation of the genital papilla with the adult coat being slightly lighter than normal. Homozygous mutant mice also have dark genitalia and a markedly diluted coat and mild macrocytic anemia.
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 000661 C3H/HeSnJ | ||
| Considerations for Choosing Controls | ||
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 003252 C57BL/6J-KitlSl-20J/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-con/Kitl+
either: (involves: C3H/HeJ) or (involves: C3H/HeN)
- pigmentation phenotype
- abnormal skin pigmentation (MGI Ref ID J:23593)
- hyperpigmentation (MGI Ref ID J:23593)
- hyperpigmentation of the genital papillae
- reproductive system phenotype
- *normal* reproductive system phenotype (MGI Ref ID J:23593)
- both males and females were fertile
- decreased oocyte cell number (MGI Ref ID J:23593)
- skin/coat/nails phenotype
- *normal* skin/coat/nails phenotype (MGI Ref ID J:23593)
- normal coat color
- abnormal skin pigmentation (MGI Ref ID J:23593)
KitlSl-con/KitlSl-con
either: (involves: C3H/HeJ) or (involves: C3H/HeN)
- pigmentation phenotype
- abnormal coat/hair pigmentation (MGI Ref ID J:23593)
- uniformly gray coat
- abnormal skin pigmentation (MGI Ref ID J:23593)
- hyperpigmentation (MGI Ref ID J:23593)
- hyperpigmentation of the genitals
- occasional abnormal pigmentation of regions of the oviduct due to the accumulation of melanocytes
- endocrine/exocrine gland phenotype
- impaired ovarian folliculogenesis (MGI Ref ID J:23593)
- follicular development is initially delayed, and although follicular development is relatively normal around 4 weeks of age, follicles fail to be maintained after 5 weeks of age
- hematopoietic system phenotype
- increased mast cell number (MGI Ref ID J:23593)
- accumulation of mast cells in the reproductive tract, with the highest degree of accumulation in the serosal membrane
- immune system phenotype
- increased mast cell number (MGI Ref ID J:23593)
- accumulation of mast cells in the reproductive tract, with the highest degree of accumulation in the serosal membrane
- reproductive system phenotype
- *normal* reproductive system phenotype (MGI Ref ID J:23593)
- no defects were observed in the postnatal testes
- decreased oocyte cell number (MGI Ref ID J:23593)
- impaired ovarian folliculogenesis (MGI Ref ID J:23593)
- follicular development is initially delayed, and although follicular development is relatively normal around 4 weeks of age, follicles fail to be maintained after 5 weeks of age
- skin/coat/nails phenotype
- abnormal coat/hair pigmentation (MGI Ref ID J:23593)
- uniformly gray coat
- abnormal skin pigmentation (MGI Ref ID J:23593)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:KitlSl-con related
Cancer Research
Growth Factors/Receptors/Cytokines
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
testicular teratomas
Research Tools
Immunology and Inflammation Research
Mast Cell Deficiency
Sensorineural Research
Vestibular and Hearing Defects
| Allele Symbol | KitlSl-con | ||
|---|---|---|---|
| Allele Name | contrasted | ||
| Allele Type | Radiation induced | ||
| Common Name(s) | Mgf; | ||
| 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 |
The contrasted mutation was found in a neutron irradiation experiment. Heterozygotes are recognizable soon after birth by dark pigmentation of the genital papilla. The adult coat is slightly lighter than normal. Homozygotes also have dark external genitalia but a markedly diluted coat; they have a mild macrocytic anemia. Males are fertile but females are usually sterile (J:20215). The mutation was shown to be allelic to steel by linkage and complementation tests (J:13654). The cause of the Kitl | ||
| Molecular Note | Pulse field gel electrophoresis using cDNA and genomic clones showed that this allele is an undefined rearrangement between 90 and 2.2Mb 5' to Kitl. Northern analysis showed that the mRNA transcript is of normal size but this allele exerts tissue-specific effects on transcript abundance. [MGI Ref ID J:23593] | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Genotyping resources and troubleshooting
Arguello F; Furlanetto RW; Baggs RB; Graves BT; Harwell SE; Cohen HJ; Frantz CN. 1992. Incidence and distribution of experimental metastases in mutant mice with defective organ microenvironments (genotypes Sl/Sld and W/Wv). Cancer Res 52(8):2304-9. [PubMed: 1559233] [MGI Ref ID J:468]
Hayashi C; Sonoda T; Nakano T; Nakayama H; Kitamura Y. 1985. Mast-cell precursors in the skin of mouse embryos and their deficiency in embryos of Sl/Sld genotype. Dev Biol 109(1):234-41. [PubMed: 3987963] [MGI Ref ID J:7810]
Huang E; Nocka K; Beier DR; Chu TY; Buck J; Lahm HW; Wellner D; Leder P; Besmer P. 1990. The hematopoietic growth factor KL is encoded by the Sl locus and is the ligand of the c-kit receptor, the gene product of the W locus. Cell 63(1):225-33. [PubMed: 1698557] [MGI Ref ID J:10751]
Murphy ED. 1977. Effects of mutant steel alleles on leukemogenesis and life-span in the mouse. J Natl Cancer Inst 58(1):107-10. [PubMed: 319242] [MGI Ref ID J:5758]
Schrott A; Egg G; Spoendlin H. 1988. Intermediate filaments in the cochleas of normal and mutant (w/wv, sl/sld) mice. Arch Otorhinolaryngol 245(4):250-4. [PubMed: 2460075] [MGI Ref ID J:9423]
Schrott A; Spoendlin H. 1987. Pigment anomaly-associated inner ear deafness. Acta Otolaryngol (Stockh) 103(5-6):451-7. [PubMed: 3618172] [MGI Ref ID J:8813]
Wolf NS. 1978. Dissecting the hematopoietic microenvironment. II. The kinetics of the erythron of the S1/S1d mouse and the dual nature of its anemia. Cell Tissue Kinet 11(4):325-34. [PubMed: 688326] [MGI Ref ID J:6031]
Zsebo KM; Williams DA; Geissler EN; Broudy VC; Martin FH; Atkins HL; Hsu RY; Birkett NC; Okino KH; Murdock DC; Jacobsen FW; Langley KE; Smith KA; Takeishi T; Cattanach BM; Galli SJ; Suggs SV. 1990. Stem cell factor is encoded at the Sl locus of the mouse and is the ligand for the c-kit tyrosine kinase receptor. Cell 63(1):213-24. [PubMed: 1698556] [MGI Ref ID J:10750]
KitlSl-con relatedBedell MA; Brannan CI; Evans EP; Copeland NG; Jenkins NA; Donovan PJ. 1995. DNA rearrangements located over 100 kb 5' of the Steel (Sl)-coding region in Steel-panda and Steel-contrasted mice deregulate Sl expression and cause female sterility by disrupting ovarian follicle development. Genes Dev 9(4):455-70. [PubMed: 7533739] [MGI Ref ID J:23593]
Cattanach BM; Rasberry C. 1988. A new steel allele with early post-implantation homozygous lethality Mouse News Lett 80:157-58. [MGI Ref ID J:18280]
Kelly EM. 1974. Cloud-gray is an allele of Sl Mouse News Lett 50:52. [MGI Ref ID J:13654]
Peters J. 1987. A new steel allele which does not lead to dilution of coat colour Mouse News Lett 77:125-6. [MGI Ref ID J:24739]
Searle AG. 1968. New mutant (Contrasted) Mouse News Lett 38:22. [MGI Ref ID J:20215]
van Buul PP; Tuinenburg-Bol Raap A; Goudzwaard HJ; Seelen CM; Beechey CV; Natarajan AT; Searle AG. 1991. Cytogenetic characterization of radiosensitive mouse mutants. Mutat Res 251(2):171-9. [PubMed: 1720867] [MGI Ref ID J:4646]
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 |
|
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 |
|
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 |
|
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 000661 C3H/HeSnJ | ||
| Considerations for Choosing Controls | ||
| USA, Canada and Mexico - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
| International - Control Pricing Information for Genetically Engineered Mutant Strains. | ||
Purchasing Information
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Contact Information
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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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