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Former Names A.B6 Tyr+-Spnb4nmf261/J (Changed: 19-MAY-06 ) A.B6 Tyr+-nmf261/J (Changed: 08-AUG-05 ) NMF261 (Changed: 31-JAN-05 ) Type Chemically Induced Mutation; Mutant Strain; Additional information on Genetically Engineered Mutant Mice. Species laboratory mouse Appearance
brown
Related Genotype: a/a Tyrp1b/Tyrp1bDescription
View strain phenotype and additional information on the Neuroscience Mutagenesis Facility web page for Spnb4qv-7J entry.
| Control | ||
|---|---|---|
| +/? untyped from the colony | ||
| Considerations for Choosing Controls | ||
Strains carrying other alleles of Spnb4
001769 B6.B10Sn-Spnb4qv-lnd/J 005753 B6;CByJ-Spnb4qv-9J/J 002996 B6ByJ;D2-Spnb4qv-4J/J 000638 C3FeB6 A/Aw-J-Spnb4qv-J/J 002433 C3H/HeJ-Spnb4qv-lnd2J/J 008522 C57BL/6J-Spnb4qv-11J/J 001028 C57BL/6J-Spnb4qv-3J/J 005449 C57BL/6J-Spnb4qv-8J/J 008521 C;B6-Spnb4qv-10J/J View Strains carrying other alleles of Spnb4 (9 strains)
Genetic Quality Control Annual Report
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
Spnb4qv-7J/Spnb4qv-7J
A.B6-Tyr+/J
- muscle phenotype
- *normal* muscle phenotype (MGI Ref ID J:82238)
- pathological examination revealed no abnormalities in muscles of mice ages 43, 49 or 88 days
- whole muscle mounts of the hindlimb of an 88 day-old mouse stained with bungarotoxin, SV2 and SM31 appeared normal
- muscle weakness (MGI Ref ID J:82238)
- mutant mice from the age of 4 weeks have difficulty supporting weight on their hindlimbs and drag them intermittently
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Spnb4qv-7J related
Developmental Biology Research
Growth Defects
Neurobiology Research
Ataxia (Movement) Defects
Neuromuscular Defects
Neuroscience Mutagenesis Facility Strain
| Allele Symbol | Spnb4qv-7J | ||
|---|---|---|---|
| Allele Name | quivering 7 Jackson | ||
| Allele Type | Chemically induced (ENU) | ||
| Common Name(s) | NMF261; Spnb4nmf261; neuroscience mutagenesis facility, 261; | ||
| Strain of Origin | A.B6-Tyr+/J | ||
| Gene Symbol and Name | Spnb4, spectrin beta 4 | ||
| Chromosome | 7 | ||
| Gene Common Name(s) | 1700022P15Rik; 5830426A08Rik; KIAA1642; QV; RIKEN cDNA 1700022P15 gene; RIKEN cDNA 5830426A08 gene; ROSA62; SPTBN3; SpbIV; dyn; lnd; lumbosacral neuroaxonal dystrophy; neuroaxonal dystrophy; neuroscience mutagenesis facility, 261; neuroscience mutagenesis facility, 379; nmf261; nmf379; quivering; qv; | ||
| Molecular Note | This phenotypic mutation was identified in an ENU mutagenesis screen and shown to be an allele of Spnb4 by complementation testing versus the lumbosacral neuroaxonal dystrophy mutation of this gene. [MGI Ref ID J:82238] | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Optimizing PCR Protocols
Spnb4qv-7J relatedJAX Neuroscience Mutagenesis Facility URL: http://www.jax.org/nmf. 2003. Heritable mouse mutants from JAX NMF ENU Mutagenesis Program MGI Direct Data Submission :. [MGI Ref ID J:82238]
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 | ||
|---|---|---|
| +/? untyped 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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Technical Support Email Form
| phone: | 207-288-6470 |
| fax: | 207-288-6655 |
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