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Type Congenic; Mutant Strain; Additional information on Genetically Engineered Mutant Mice. Species laboratory mouse and M. m. castaneus Generation N36 (08-JAN-04) Appearance
black
Related Genotype: a/a
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| Considerations for Choosing Controls | ||
Strains carrying Gpi1a allele
000600 B6-Gpi1b x B6CBCa Aw-J/A-T(7;15)9H Gpi1a/J 000377 B6.C-H22c Gpi1a/(HW38)ByJ 000123 B6.C-H24c Gpi1a/(HW54)ByJ 000797 B6.CAST-Gpi1a/EiJ 002074 B6.Cg-Gpi1a Hbbd H1b/DehJ 001317 B6.Cg-Igha Thy1a Gpi1a/J 000909 B6CBy-Gpi1a/Gpi1b/J or Gpi1a-m1/Gpi1b/J 002800 C3.Cg-Gpi1a/J View Strains carrying Gpi1a (8 strains)
Strains carrying Hbath-J allele
000802 WB.Cg-Hbath-J/J View Strains carrying Hbath-J (1 strain)
Strains carrying other alleles of Gpi1
View Strains carrying other alleles of Gpi1 (8 strains)
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 Related Disease (OMIM) Terms
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
Hbath-J/Hba+
involves: C57BL/6J
- lethality-postnatal
- postnatal lethality (MGI Ref ID J:32654)
- fewer than expected heterozygous mice are found at weaning (39% compared to the expected 50%)
- growth/size phenotype
- decreased body weight (MGI Ref ID J:45721)
- hematopoietic system phenotype
- decreased hemoglobin content (MGI Ref ID J:45721)
- low blood hemoglobin levels
- increased erythrocyte cell number (MGI Ref ID J:45721)
- erythrocytosis
- microcytosis (MGI Ref ID J:45721)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:
Gpi1a relatedHematological Research
Hemoglobin Defects (thalassemia)
Hbath-J relatedImmunology and Inflammation Research
CD Antigens, Antigen Receptors, and Histocompatibility Markers
Research Tools
Genetics Research (Tissue/Cell Markers)
Developmental Biology Research
Embryonic Lethality (Homozygous)
Hematological Research
Hemoglobin Defects
| Allele Symbol | Gpi1a | ||
|---|---|---|---|
| Allele Name | a variant | ||
| Allele Type | Not Applicable | ||
| Gene Symbol and Name | Gpi1, glucose phosphate isomerase 1 | ||
| Chromosome | 7 | ||
| Gene Common Name(s) | AMF; GNPI; Gpi-1; Gpi-1r; Gpi-1s; Gpi-1t; Gpi1-r; Gpi1-s; Gpi1-t; MF; NK; NK/GPI; NLK; Org; PGI; PHI; SA-36; autocrine motility factor; glucose phosphate isomerase 1, regulatory; glucose phosphate isomerase 1, structural; glucose phosphate isomerase 1, temporal; maturation factor; neuroleukin; | ||
| Molecular Note | This allele determines a slower migrating variant of the encoded enzyme and occurs in the wild and in strains A/HeJ, AKR/J, BALB/cJ, C57BR/cdJ, C58/J, CE/J, DBA/2J, DE/J, DW/J, LP/J, MA/J, NZB, PL/J, P/J, RARF, RF/J, SJL/J, ST/bJ, and 129/J. Sequencing analysis identified four nucleotide differences between this allele and Gpi1b. Two differences were silent, while a third difference at position 282 predicts an aspartate for the a allele and an asparagine for the b allele. A fourth difference in the 3' untranslated region was also noted. [MGI Ref ID J:28033] | ||
| 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
Gpi1a relatedHbath-J relatedCharles DJ; Lee CY. 1980. Biochemical and immunological characterization of genetic variants of phosphoglucose isomerase from mouse. Biochem Genet 18(1-2):153-69. [PubMed: 6155905] [MGI Ref ID J:6330]
Chen J; Reifsnyder PC; Scheuplein F; Schott WH; Mileikovsky M; Soodeen-Karamath S; Nagy A; Dosch MH; Ellis J; Koch-Nolte F; Leiter EH. 2005. 'Agouti NOD': identification of a CBA-derived Idd locus on Chromosome 7 and its use for chimera production with NOD embryonic stem cells. Mamm Genome 16(10):775-83. [PubMed: 16261419] [MGI Ref ID J:102639]
Chen TT; Li L; Chung DH; Allen CD; Torti SV; Torti FM; Cyster JG; Chen CY; Brodsky FM; Niemi EC; Nakamura MC; Seaman WE; Daws MR. 2005. TIM-2 is expressed on B cells and in liver and kidney and is a receptor for H-ferritin endocytosis. J Exp Med 202(7):955-65. [PubMed: 16203866] [MGI Ref ID J:107466]
Collinson JM; Quinn JC; Hill RE; West JD. 2003. The roles of Pax6 in the cornea, retina, and olfactory epithelium of the developing mouse embryo. Dev Biol 255(2):303-12. [PubMed: 12648492] [MGI Ref ID J:82632]
DeLorenzo RJ; Ruddle FH. 1969. Genetic control of two electrophoretic variants of glucosephosphate isomerase in the mouse (Mus musculus). Biochem Genet 3(2):151-62. [PubMed: 5364923] [MGI Ref ID J:5141]
Ito CY; Li CY; Bernstein A; Dick JE; Stanford WL. 2003. Hematopoietic stem cell and progenitor defects in Sca-1/Ly-6A-null mice. Blood 101(2):517-23. [PubMed: 12393491] [MGI Ref ID J:81387]
Pearce SR; Morgan MJ; Ball S; Peters J; Faik P. 1995. Sequence characterization of alleles Gpi1-Sa and Gpi1-Sb at the glucose phosphate isomerase structural locus. Mamm Genome 6(8):537-9. [PubMed: 8589524] [MGI Ref ID J:28033]
Szuber N; Buss JL; Soe-Lin S; Felfly H; Trudel M; Ponka P. 2008. Alternative treatment paradigm for thalassemia using iron chelators. Exp Hematol 36(7):773-85. [PubMed: 18456387] [MGI Ref ID J:136991]
Chang 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 |
|
*Price(s) in US dollars ($)
Weeks of Age Price* Gender Cryorecovery Fee $1900.00
| Pricing for International shipping destinations |
|
*Price(s) in US dollars ($)
Weeks of Age Price* Gender 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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| 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. | ||
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