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Type Chemically Induced Mutation; Congenic; Mutant Strain; Additional information on Genetically Engineered Mutant Mice. Species laboratory mouse Background Strain WB/Re Donor Strain B6 x TEM treated PosA male (derived from M. m. poschiavinus and Swiss mice) Generation N33p
Strains carrying Hbath-J allele
001622 B6.CAST-Gpi1a.Cg-Hbath-J View Strains carrying Hbath-J (1 strain)
Strains carrying other alleles of Hba
002616 B6.129S7-Hbatm1Paz/J 003342 STOCK Hbatm1Paz Hbbtm1Tow Tg(HBA-HBBs)41Paz/J View Strains carrying other alleles of Hba (2 strains)
Congenic Nomenclature
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Hbath-J relatedHematological Research
Hemoglobin Defects (thalassemia)
Developmental Biology Research
Embryonic Lethality (Homozygous)
Hematological Research
Hemoglobin Defects
| Allele Symbol | Hbath-J | ||
|---|---|---|---|
| Allele Name | alpha thalassemia Jackson | ||
| Allele Type | Chemically induced (other) | ||
| Common Name(s) | alphaMD; | ||
| Strain of Origin | C57BL/6J x Triethyllenemelamine-treated male | ||
| Gene Symbol and Name | Hba, hemoglobin alpha chain complex | ||
| Chromosome | 11 | ||
| General Note | The mutation was induced in a male mouse by triethyllenemelamine. | ||
| Molecular Note | This mutation was shown to be a deletion that included the Hba-x, Hba-a1 and Hba-a2 genes (J:32654). The Mpg, Rhbdf1 and Phg genes are also included in the deletion region (J:29665). [MGI Ref ID J:29665] [MGI Ref ID J:32654] | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Optimizing PCR Protocols
Hbath-J relatedChang J; Lu RH; Xu SM; Meneses J; Chan K; Pedersen R; Kan YW. 1996. Inactivation of mouse alpha-globin gene by homologous recombination: mouse model of hemoglobin H disease. Blood 88(5):1846-51. [PubMed: 8781443] [MGI Ref ID J:35018]
Fabry ME; Costantini F; Pachnis A; Suzuka SM; Bank N; Aynedjian HS; Factor SM; Nagel RL. 1992. High expression of human beta S- and alpha-globins in transgenic mice: erythrocyte abnormalities, organ damage, and the effect of hypoxia. Proc Natl Acad Sci U S A 89(24):12155-9. [PubMed: 1465455] [MGI Ref ID J:129537]
Fabry ME; Nagel RL; Pachnis A; Suzuka SM; Costantini F. 1992. High expression of human beta S- and alpha-globins in transgenic mice: hemoglobin composition and hematological consequences. Proc Natl Acad Sci U S A 89(24):12150-4. [PubMed: 1465454] [MGI Ref ID J:129579]
Fabry ME; Sengupta A; Suzuka SM; Costantini F; Rubin EM; Hofrichter J; Christoph G; Manci E; Culberson D; Factor SM; et al.. 1995. A second generation transgenic mouse model expressing both hemoglobin S (HbS) and HbS-Antilles results in increased phenotypic severity. Blood 86(6):2419-28. [PubMed: 7662990] [MGI Ref ID J:94190]
Hendrey J; Lin D; Dziadek M. 1995. Developmental analysis of the Hba(th-J) mouse mutation: effects on mouse peri-implantation development and identification of two candidate genes. Dev Biol 172(1):253-63. [PubMed: 7589805] [MGI Ref ID J:29665]
Hendrey JA; Dziadek M. 1995. Effects on neonatal growth of the Hba(th-j) deletion on mouse chromosome 11 are not due to genomic imprinting. Growth Regul 5(3):160-3. [PubMed: 7580867] [MGI Ref ID J:29127]
Whitney JB 3d; Martinell J; Popp RA; Russell LB; Anderson WF. 1981. Deletions in the alpha-globin gene complex in alpha-thalassemic mice. Proc Natl Acad Sci U S A 78(12):7644-7. [PubMed: 6950407] [MGI Ref ID J:32654]
Whitney JB 3d; Popp RA. 1984. Animal model of human disease: thalassemia: alpha-thalassemia in laboratory mice. Am J Pathol 116(3):523-5. [PubMed: 6476083] [MGI Ref ID J:7581]
Whitney JB 3d; Russell ES. 1980. Linkage of genes for adult alpha-globin and embryonic alpha-like globin chains. Proc Natl Acad Sci U S A 77(2):1087-90. [PubMed: 6153802] [MGI Ref ID J:6282]
Whitney JB; Russell ES. 1978. New mutants and biochemical variants: Alpha thalassemia Mouse News Lett 58:47-48. [MGI Ref ID J:45721]
Yu X; Kong Y; Dore LC; Abdulmalik O; Katein AM; Zhou S; Choi JK; Gell D; Mackay JP; Gow AJ; Weiss MJ. 2007. An erythroid chaperone that facilitates folding of alpha-globin subunits for hemoglobin synthesis. J Clin Invest 117(7):1856-65. [PubMed: 17607360] [MGI Ref ID J:124209]
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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*Price(s) in US dollars ($)
Price* Cryorecovery Fee $1900.00
| Pricing for International shipping destinations |
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*Price(s) in US dollars ($)
Price* Cryorecovery Fee $2470.00
| Standard Supply | Repository-Cryopreserved. Must Be Recovered. Please refer to pricing and supply notes for further information. |
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| Supply Notes |
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