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Type Segregating Inbred; Type Mutant Strain; Spontaneous Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Mating System Heterozygote x +/+ sibling (Female x Male) 27-NOV-07 Mating System +/+ sibling x Heterozygote (Female x Male) 27-NOV-07 Species laboratory mouse H2 Haplotype j Generation F187 (03-JAN-08)
View larger imageAppearance
diluted black with white belly spot, occasionally has white head blaze, tail has white tip, affected
Related Genotype: a/a KitW/+
non-diluted black, frequently have small belly spots, unaffected
Related Genotype: a/a +/+Important Note
This strain is homozygous for the retinal degeneration allele Pde6brd1. See article "Genetic Background Effects: Can Your Mice See?", JAX® NOTES Spring 2002, No. 485.Description
Kit mice possess pleiotropic defects in pigment-forming cells, germ cells, RBC's and mast cells. In addition, they exhibit impaired resistance to parasitic infection and an intrinsic progenitor cell defect. The lack of germ cells in homozygous mutant mice leads to the development of some ovarian tumors (mesotheliomas and granulosa cell), associated with an overproduction of pituitary gonadotropic hormone.
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| Considerations for Choosing Controls | ||
Strains carrying KitW allele
000164 B6.Cg-KitW/J 000092 FL/1Re-KitW/J 100410 WBB6F1/J-KitW/KitW-v/J View Strains carrying KitW (3 strains)
Strains carrying Pde6brd1 allele
View Strains carrying Pde6brd1 (74 strains)
Strains carrying other alleles of Kit
000599 B6 x B6CBCa Aw-J/A-T(5;13)264Ca KitW-v/J 006564 B6(C)-KitW-41J Gusbmps/BrkJ 000495 B6.C-H38c/By-KitW-56J/J 000560 B6.C-H7b/By KitW-50J/J 000122 B6.C3-KitW-44J/J 000991 B6.C58-KitW-57J/J 002283 B6.Cg-KitW-19H/EiJ 000133 B6.Cg-KitW-24J/J 000139 B6.Cg-KitW-25J/J 005051 B6.Cg-KitW-sh/HNihrJaeBsmJ 000194 B6.Cg-Lx KitW-v/J 000171 B6.D2-KitW-45J/J 001563 B6.D2-KitW-73J/J 001177 B6.LP-KitW-49J/J 000350 B6By.Cg-KitW-v MitfMi-wh T/J 000627 C3H/HeJ-KitW-x/J 000847 C3Sn.B6-KitW-39J/J 000166 C57BL/6J-KitW-17J/J 000167 C57BL/6J-KitW-18J/J 000169 C57BL/6J-KitW-20J/J 000117 C57BL/6J-KitW-34J/J 000128 C57BL/6J-KitW-35J/J 000134 C57BL/6J-KitW-37J/J 000062 C57BL/6J-KitW-39J/J 000121 C57BL/6J-KitW-40J/J 000119 C57BL/6J-KitW-41J/J 000127 C57BL/6J-KitW-42J/J 000129 C57BL/6J-KitW-43J/J 000990 C57BL/6J-KitW-55J/J 001179 C57BL/6J-KitW-62J/J 000049 C57BL/6J-KitW-v/J 000965 CBACa.C3-KitW-x/J 000993 NZB/BlNJ-KitW-59J/J 100410 WBB6F1/J-KitW/KitW-v/J View Strains carrying other alleles of Kit (34 strains)
Strains carrying other alleles of Pde6b
004297 B6.CXB1-Pde6brd10/J 003647 B6EiC3Sn.BLiAF1 002802 C3.BLiA Pde6b+-Krd/J 001979 C3A.BLiA-Pde6b+.O20-Prph2Rd2/J 001912 C3A.BLiA-Pde6b+/J 003648 C3Sn.BLiA-Pde6b+/Dn 004766 C57BL/6J-Pde6brd1-2J/J 004828 FVB.129P2-Pde6b+ Tyrc-ch/AntJ 004808 STOCK Mapttm1(EGFP)Klt Tg(MAPT)8cPdav/J View Strains carrying other alleles of Pde6b (9 strains)
Genetic Quality Control Annual Report
JAX® NOTES, April 1988; 433. H-2 Haplotypes of Mice from Jackson Laboratory Production Colonies.
JAX® NOTES, Spring 2002; 485. Genetic Background Effects: Can Your Mice See?
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
KitW/Kit+
Background Not Specified
- pigmentation phenotype
- abnormal coat/hair pigmentation (MGI Ref ID J:12955)
- irregular coat pigmentation (MGI Ref ID J:12955)
- pigmented areas of the coat may be interspersed with white hairs producing a roan appearance pigmented coat may be interspersed with white hairs creating a roan appearance pigmented areas are interspersed with white hairs producing a roan appearance
- variable body spotting (MGI Ref ID J:12955)
- variable amounts of white spotting
- hematopoietic system phenotype
- *normal* hematopoietic system phenotype (MGI Ref ID J:14978)
- blood parameters are normal
- skin/coat/nails phenotype
- abnormal coat/hair pigmentation (MGI Ref ID J:12955)
- irregular coat pigmentation (MGI Ref ID J:12955)
- pigmented areas of the coat may be interspersed with white hairs producing a roan appearance pigmented coat may be interspersed with white hairs creating a roan appearance pigmented areas are interspersed with white hairs producing a roan appearance
- variable body spotting (MGI Ref ID J:12955)
- variable amounts of white spotting
- reproductive system phenotype
- *normal* reproductive system phenotype (MGI Ref ID J:14978)
- system is normal
KitW/KitW
Background Not Specified
- lethality-postnatal
- postnatal lethality (MGI Ref ID J:12955)
- death is within the first week of birth
- hematopoietic system phenotype
- macrocytic anemia (MGI Ref ID J:14978)
- macrocytic anemia begins at 12 days gestation leading to death within the first week of birth
- pigmentation phenotype
- abnormal eye pigmentation (MGI Ref ID J:12955)
- pigment is restricted to retina
- absent coat pigmentation (MGI Ref ID J:12955)
- white coat color, vividly contrasts with normal black eye color
- skin/coat/nails phenotype
- absent coat pigmentation (MGI Ref ID J:12955)
- white coat color, vividly contrasts with normal black eye color
- vision/eye phenotype
- abnormal eye pigmentation (MGI Ref ID J:12955)
- pigment is restricted to retina
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
KitW relatedSensorineural Research
Retinal Degeneration
Pde6brd1
Pde6brd1 relatedCancer Research
Growth Factors/Receptors/Cytokines
Increased Tumor Incidence
Gonadal Tumors: ovarian
Oncogenes
Dermatology Research
Color and White Spotting Defects
Developmental Biology Research
Neural Crest Defects
Endocrine Deficiency Research
Bone/Bone Marrow Defects
Gonad Defects
Skin Defects
Immunology and Inflammation Research
Immunodeficiency
Mast Cell Deficiency
Mouse/Human Gene Homologs
piebaldism
synpolydactyly
Neurobiology Research
Receptor Defects
Vestibular and Hearing Defects
Reproductive Biology Research
Developmental Defects Affecting Gonads
germ cell deficient
Fertility Defects
Gonadal Tumors
ovarian
Research Tools
Immunology and Inflammation Research
Mast Cell Deficiency
Sensorineural Research
Retinal Degeneration
Vestibular and Hearing Defects
Mouse/Human Gene Homologs
retinitis pigmentosa, autosomal recessive
Sensorineural Research
Retinal Degeneration
| Allele Symbol | KitW | ||
|---|---|---|---|
| Allele Name | dominant spotting | ||
| Allele Type | Spontaneous | ||
| Common Name(s) | W; | ||
| Strain of Origin | old mutant of the mouse fancy | ||
| Gene Symbol and Name | Kit, kit oncogene | ||
| Chromosome | 5 | ||
| Gene Common Name(s) | Bs; C-Kit; CD117; Dominant white spotting; Fdc; Gsfsco1; Gsfsco5; Gsfsow3; PBT; SCFR; SCO1; SCO5; SOW3; Ssm; Steel Factor Receptor; Tr-kit; W; belly-spot; dominant spotting; gsf spotted coat 1; gsf spotted coat 5; phenotype like Sl or W 3; spotted sterile male; | ||
| General Note | This is an old mutant of the mouse fancy. KitW mutants are a potential model for human inherited pure red cell anemia, called Diamond-Blackfan anemia (OMIM 205900), but mouse mutants do not respond to corticosteroid treatment as do human patients. Thus, the mechanism of anemia causation in the two conditions must be different (J:14286). | ||
| Molecular Note | A guanosine to adenosine substitution at the first nucleotide at the 5' boundary of the intron following the transmembrane exon results in two different aberrantly spliced transcripts putatively expressed in a tissue specific manner. A deletion of 107 bp was found in transcripts from mast cells of mutant mice. A deletion of 234 was found in transcripts from brain or bone marrow cells. The GT to AT point mutation probably disrupted a splice donor site, thereby causing exon skipping. The 107 bp deletion could have resulted from skipping of a transmembrane region exon and the 234 bp deletion from skipping 3 exons. The 107 bp deletion would generate a stop codon 12 bp downstream because of a frame shift, whereas the larger deletion would still be in frame. Northern blot analysis indicated that mast cells from mutants have only 31-37% of the transcripts as mast cells derived from normal bone marrow, suggesting that the mutation may reduce efficiency and authenticity of transcription and splicing. [MGI Ref ID J:91867] | ||
| Allele Symbol | Pde6brd1 | ||
| Allele Name | retinal degeneration 1 | ||
| Allele Type | Spontaneous | ||
| Common Name(s) | Pdebrd1; rd; rd-1; rd1; rodless retina; | ||
Genotyping Protocols
KitW, Pyrosequencing
Helpful Links
Genotyping resources and troubleshooting
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Ayach BB; Yoshimitsu M; Dawood F; Sun M; Arab S; Chen M; Higuchi K; Siatskas C; Lee P; Lim H; Zhang J; Cukerman E; Stanford WL; Medin JA; Liu PP. 2006. Stem cell factor receptor induces progenitor and natural killer cell-mediated cardiac survival and repair after myocardial infarction. Proc Natl Acad Sci U S A 103(7):2304-9. [PubMed: 16467148] [MGI Ref ID J:106065]
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Ito A; Jippo T; Wakayama T; Morii E; Koma Y; Onda H; Nojima H; Iseki S; Kitamura Y. 2003. SgIGSF: a new mast-cell adhesion molecule used for attachment to fibroblasts and transcriptionally regulated by MITF. Blood 101(7):2601-8. [PubMed: 12456501] [MGI Ref ID J:115530]
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Tsujimura Y; Obata K; Mukai K; Shindou H; Yoshida M; Nishikado H; Kawano Y; Minegishi Y; Shimizu T; Karasuyama H. 2008. Basophils play a pivotal role in immunoglobulin-G-mediated but not immunoglobulin-E-mediated systemic anaphylaxis. Immunity 28(4):581-9. [PubMed: 18342553] [MGI Ref ID J:134463]
Wang CH; Anderson N; Li SH; Szmitko PE; Cherng WJ; Fedak PW; Fazel S; Li RK; Yau TM; Weisel RD; Stanford WL; Verma S. 2006. Stem cell factor deficiency is vasculoprotective: unraveling a new therapeutic potential of imatinib mesylate. Circ Res 99(6):617-25. [PubMed: 16931795] [MGI Ref ID J:125065]
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Animal Health Reports
Room Number AX5
Colony Maintenance
Breeding & Husbandry Wildtype mice from this colony frequently show small belly spots on an otherwise non-diluted black background. Attempts to breed away from this phenotype can reduce the incidence, but can not fully eliminate it. Mating System Heterozygote x +/+ sibling (Female x Male) 27-NOV-07 +/+ sibling x Heterozygote (Female x Male) 27-NOV-07 Diet Information LabDiet® 5K52/5K67
| Pricing for USA, Canada and Mexico shipping destinations |
|
Weeks of Age Price (US dollars $) Gender Genotypes Provided 3-5 weeks $104.55 Female or Male Heterozygous for KitW 6 weeks $107.20 Female or Male Heterozygous for KitW 7 weeks $109.85 Female or Male Heterozygous for KitW 8 weeks $112.50 Female or Male Heterozygous for KitW
Pairs /Price (US dollars $) Pair Genotype $161.55 Heterozygous for KitW x Wild-type for KitW
| Pricing for International shipping destinations |
|
Weeks of Age Price (US dollars $) Gender Genotypes Provided 3-5 weeks $136.00 Female or Male Heterozygous for KitW 6 weeks $139.50 Female or Male Heterozygous for KitW 7 weeks $143.00 Female or Male Heterozygous for KitW 8 weeks $146.50 Female or Male Heterozygous for KitW
Pairs /Price (US dollars $) Pair Genotype $210.10 Heterozygous for KitW x Wild-type for KitW
| Standard Supply | Level 4. Up to 10 mice. Larger quantities or custom orders arranged upon request. Expected delivery up to one to three months. |
|---|---|
| Supply Notes |
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| Important Note | |
| This strain is homozygous for the retinal degeneration allele Pde6brd1. See article "Genetic Background Effects: Can Your Mice See?", JAX® NOTES Spring 2002, No. 485. | |
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 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
JAX® Mice Orders
Surgical Services
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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