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Type Congenic; Mutant Strain; Targeted Mutation; Additional information on Genetically Engineered Mutant Mice. Species laboratory mouse Donating Investigator Thomas Schwarz, Harvard University Description
Mice that are homozygous for the targeted mutation are viable, fertile, normal in size and do not display any gross physical or behavioral abnormalities. No gene product (mRNA or protein) is detected by Northern blot analysis of cardiac tissue or Southern blot analysis. Cardiac ventribular myocytes isolated from homozygotes exhibit a 50% reduction in inwardly rectifying potassium ion currents under physiological and elevated extracellular potassium ion concentration levels. This mutant mouse strain may be useful in studies of potassium ion dependent cardiac electrophysiology.Development
A targeting vector containing neomycin resistance and herpes simplex virus thymidine kinase genes was used to disrupt the entire open reading frame. The construct was electroporated into 129-derived R1 embryonic stem (ES) cells. Correctly targeted ES cells were injected into C57BL/6 blastocysts.
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 001800 FVB/NJ | ||
| Considerations for Choosing Controls | ||
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
Kcnj12tm1Swz/Kcnj12tm1Swz
involves: 129S1/Sv * 129X1/SvJ * FVB
- cardiovascular system phenotype
- *normal* cardiovascular system phenotype (MGI Ref ID J:78077)
- the hearts and brains of homozygous null mice displayed no morphological or histological abnormalities
- cerebral arteries from wild-type and homozygous null mice constricted to the same degree to intravascular pressure (80 mm Hg)
- Ba2+-sensitive K+-induced dilations were similar in pressurized cerebral arteries from wild-type and homozygous null adult mice; both control and homozygous null arteries dilated when the extracellular K+ concentration was increased from 6 to 15 mmol/L
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Kcnj12tm1Swz related
Cardiovascular Research
Heart Abnormalities
Cell Biology Research
Channel and Transporter Defects (potassium)
| Allele Symbol | Kcnj12tm1Swz | ||
|---|---|---|---|
| Allele Name | targeted mutation 1, Thomas L Schwarz | ||
| Allele Type | Targeted (knock-out) | ||
| Common Name(s) | Kir2.2-/-; | ||
| Mutation Made By | Joshua Zaritsky, Harvard University | ||
| Strain of Origin | (129X1/SvJ x 129S1/Sv)F1-Kitl+ | ||
| ES Cell Line Name | R1 | ||
| ES Cell Line Strain | (129X1/SvJ x 129S1/Sv)F1-Kitl<+> | ||
| Gene Symbol and Name | Kcnj12, potassium inwardly-rectifying channel, subfamily J, member 12 | ||
| Chromosome | 11 | ||
| Gene Common Name(s) | FLJ14167; IRK2; KCNJN1; Kir2.1; Kir2.2; Kir2.2v; MB-IRK2; MGC156606; hIRK; hIRK1; hkir2.2x; kcnj12x; | ||
| Molecular Note | The entire open reading frame of the endogenous gene was deleted by the insertion of a neomycin selection cassette. [MGI Ref ID J:78077] | ||
Genotyping Protocols
Kcnj12tm1Swz, STD PCR, vers. 2
Helpful Links
Optimizing PCR Protocols
Zaritsky JJ; Eckman DM; Wellman GC; Nelson MT; Schwarz TL. 2000. Targeted disruption of Kir2.1 and Kir2.2 genes reveals the essential role of the inwardly rectifying K(+) current in K(+)-mediated vasodilation. Circ Res 87(2):160-6. [PubMed: 10904001] [MGI Ref ID J:78077]
Kcnj12tm1Swz relatedOyamada Y; Yamaguchi K; Murai M; Hakuno H; Ishizaka A. 2005. Role of Kir2.2 in hypercapnic ventilatory response during postnatal development of mouse. Respir Physiol Neurobiol 145(2-3):143-51. [PubMed: 15705530] [MGI Ref ID J:101862]
Zaritsky JJ; Redell JB; Tempel BL; Schwarz TL. 2001. The consequences of disrupting cardiac inwardly rectifying K(+) current (I(K1)) as revealed by the targeted deletion of the murine Kir2.1 and Kir2.2 genes. J Physiol 533(Pt 3):697-710. [PubMed: 11410627] [MGI Ref ID J:106468]
Colony Maintenance
Breeding & Husbandry The resulting chimeric animals were crossed to FVB mice, and then backcrossed to the same for 10 generations.
| Pricing for USA, Canada and Mexico shipping destinations |
|
*Price(s) in US dollars ($)
Weeks of Age Price* Gender Cryorecovery Fee $1900.00 Cryopreserved Embryos Fee $1600.00
| Pricing for International shipping destinations |
|
*Price(s) in US dollars ($)
Weeks of Age Price* Gender Cryorecovery Fee $2470.00 Cryopreserved Embryos Fee $2080.00
| Standard Supply | Repository-Cryopreserved. Must Be Recovered. Please refer to pricing and supply notes for further information. |
|---|---|
| Supply Notes |
|
| Control | ||
|---|---|---|
| Wild-type from the colony | ||
| 001800 FVB/NJ | ||
| 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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| phone: | 207-288-6470 |
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