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Type Coisogenic; Mutant Strain; Spontaneous Mutation; Additional information on Genetically Engineered and Mutant Mice. Visit our online Nomenclature tutorial. Species laboratory mouse Generation F85+5N8F1N1
| Control | ||
|---|---|---|
| Untyped from the colony | ||
| 000664 C57BL/6J | ||
| Considerations for Choosing Controls | ||
Strains carrying other alleles of Glra1
001278 B6C3Fe a/a-Glra1spd/J 004109 C57BL/6J-Glra1nmf11/J View Strains carrying other alleles of Glra1 (2 strains)
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
Glra1spd-ot/Glra1spd-ot
C57BL/6J-Glra1spd-ot Mpzl3rc
- lethality-postnatal
- postnatal lethality (MGI Ref ID J:13463)
- usually die about 22-23 days of age
- behavior/neurological phenotype
- tremors (MGI Ref ID J:13463)
- begin to tremble violently and very rapidly at about 14 days of age; severity of tremor increases daily
- at 19-21 days of age, mutants have prolonged periods of great rigor or stiffness; therapy with aminooxyacetic acid is helpful but only temporarily
Glra1spd-ot/Glra1spd-ot
involves: C57BL/6J
- lethality-postnatal
- postnatal lethality (MGI Ref ID J:107942)
- homozygotes die by the end of the third week after birth
- nervous system phenotype
- *normal* nervous system phenotype (MGI Ref ID J:132622)
- mice exhibit normal spontaenous glycinergic inhibitory postsynaptic currents in amacrine cells
- abnormal nervous system electrophysiology (MGI Ref ID J:107942)
- phrenic nerve discharge patterns of mutant mice vary with respect to burst frequency and duration of expiration and inspiration compared to wild-type mice; mutants displayed more frequent phrenic nerve discharges with shorter, less regular expiratory intervals
- decreased neuron number (MGI Ref ID J:107942)
- in mutants there is a reduction or absence of post-inspiratory neurons compared to wild-type
- muscle phenotype
- muscle spasm (MGI Ref ID J:107942)
- after rapid breathing episodes, single or multiple whole-body spasms occur with intervals between spasms of 6 seconds to more than 1 minute
- respiratory system phenotype
- abnormal breathing frequency (MGI Ref ID J:107942)
- conscious mutants (P16-23) display disturbed respiratory patterns characterized by periods of slow breathing and intermittent episodes of rapid breathing; episodes are of variable (2-10 sec)
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Glra1spd-ot related
Cell Biology Research
Channel and Transporter Defects (chloride: glycine receptor)
Mouse/Human Gene Homologs
Kok disease-hyperexplexia, startle disease
Neurobiology Research
Channel and Transporter Defects (chloride: glycine receptor)
Neurotransmitter Receptor and Synaptic Vesicle Defects
Receptor Defects
Tremor Defects
| Allele Symbol | Glra1spd-ot | ||
|---|---|---|---|
| Allele Name | spasmodic oscillator | ||
| Allele Type | Spontaneous | ||
| Common Name(s) | ot; | ||
| Strain of Origin | C57BL/6J-Mpzl3 | ||
| Gene Symbol and Name | Glra1, glycine receptor, alpha 1 subunit | ||
| Chromosome | 11 | ||
| Gene Common Name(s) | B230397M16Rik; GLYRA1; MGC138878; MGC138879; RIKEN cDNA B230397M16 gene; STHE; neuroscience mutagenesis facility, 11; nmf11; oscillator; ot; spasmodic; spd; | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Optimizing PCR Protocols
Buckwalter MS; Cook SA; Davisson MT; White WF; Camper SA. 1994. A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death. Hum Mol Genet 3(11):2025-30. [PubMed: 7874121] [MGI Ref ID J:21529]
Findlay GS; Phelan R; Roberts MT; Homanics GE; Bergeson SE; Lopreato GF; Mihic SJ; Blednov YA; Harris RA. 2003. Glycine receptor knock-in mice and hyperekplexia-like phenotypes: comparisons with the null mutant. J Neurosci 23(22):8051-9. [PubMed: 12954867] [MGI Ref ID J:85341]
Glra1spd-ot relatedBuckwalter MS; Cook SA; Davisson MT; White WF; Camper SA. 1994. A frameshift mutation in the mouse alpha 1 glycine receptor gene (Glra1) results in progressive neurological symptoms and juvenile death. Hum Mol Genet 3(11):2025-30. [PubMed: 7874121] [MGI Ref ID J:21529]
Busselberg D; Bischoff AM; Becker K; Becker CM; Richter DW. 2001. The respiratory rhythm in mutant oscillator mice. Neurosci Lett 316(2):99-102. [PubMed: 11742725] [MGI Ref ID J:107942]
Cook SA. 1993. Oscillator (ot) Mouse Genome 91(1):117. [MGI Ref ID J:4292]
Dickie MM. 1967. Oscillator. Mouse News Lett 36:39. [MGI Ref ID J:13463]
Findlay GS; Phelan R; Roberts MT; Homanics GE; Bergeson SE; Lopreato GF; Mihic SJ; Blednov YA; Harris RA. 2003. Glycine receptor knock-in mice and hyperekplexia-like phenotypes: comparisons with the null mutant. J Neurosci 23(22):8051-9. [PubMed: 12954867] [MGI Ref ID J:85341]
Graham BA; Schofield PR; Sah P; Callister RJ. 2003. Altered inhibitory synaptic transmission in superficial dorsal horn neurones in spastic and oscillator mice. J Physiol 551(Pt 3):905-16. [PubMed: 12837931] [MGI Ref ID J:105485]
Graham BA; Schofield PR; Sah P; Margrie TW; Callister RJ. 2006. Distinct physiological mechanisms underlie altered glycinergic synaptic transmission in the murine mutants spastic, spasmodic, and oscillator. J Neurosci 26(18):4880-90. [PubMed: 16672662] [MGI Ref ID J:108318]
Ivanova E; Muller U; Wassle H. 2006. Characterization of the glycinergic input to bipolar cells of the mouse retina. Eur J Neurosci 23(2):350-64. [PubMed: 16420443] [MGI Ref ID J:105396]
Kling C; Koch M; Saul B; Becker CM. 1997. The frameshift mutation oscillator (Glra1(spd-ot)) produces a complete loss of glycine receptor alpha1-polypeptide in mouse central nervous system. Neuroscience 78(2):411-7. [PubMed: 9145798] [MGI Ref ID J:42647]
Markstahler U; Kremer E; Kimmina S; Becker K; Richter DW. 2002. Effects of functional knock-out of alpha 1 glycine-receptors on breathing movements in oscillator mice. Respir Physiol Neurobiol 130(1):33-42. [PubMed: 12380014] [MGI Ref ID J:102716]
Simon ES. 1997. Phenotypic heterogeneity and disease course in three murine strains with mutations in genes encoding for alpha 1 and beta glycine receptor subunits. Mov Disord 12(2):221-8. [PubMed: 9087981] [MGI Ref ID J:41909]
Weiss J; O'Sullivan GA; Heinze L; Chen HX; Betz H; Wassle H. 2008. Glycinergic input of small-field amacrine cells in the retinas of wildtype and glycine receptor deficient mice. Mol Cell Neurosci 37(1):40-55. [PubMed: 17920294] [MGI Ref ID J:132622]
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. |
|---|---|
| Supply Notes |
|
| Control | ||
|---|---|---|
| Untyped from the colony | ||
| 000664 C57BL/6J | ||
| 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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Tel: 800.422.6423 or 207.288.5845
Fax: 207.288.6150
Technical Support Email Form
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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