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Former Names C57BL/6J-nmf11/J (Changed: 23-OCT-06 ) C57BL/6J-nmf11 (Changed: 15-DEC-04 ) NMF11 (Changed: 15-DEC-04 ) Type Chemically Induced Mutation; Mutant Strain; Additional information on Genetically Engineered Mutant Mice. Species laboratory mouse H2 Haplotype b Generation NE2pN1 (01-FEB-04) Appearance
black
Related Genotype: a/aDescription
View strain phenotype and additional information on the Neuroscience Mutagenesis Facility web page for Glra1nmf11 entry.
Strains carrying other alleles of Glra1
001278 B6C3Fe a/a-Glra1spd/J 000536 C57BL/6J-Glra1spd-ot/J View Strains carrying other alleles of Glra1 (2 strains)
View Mammalian Phenotype Terms
Mammalian Phenotype Terms
assigned by genotype
Glra1nmf11/Glra1nmf11
C57BL/6J-Glra1nmf11/J
- life span-post-weaning/aging
- premature death (MGI Ref ID J:78134)
- homozygotes are not viable
- adipose tissue phenotype
- decreased white adipose tissue amount (MGI Ref ID J:78134)
- little or no white fat was present
- behavior/neurological phenotype
- abnormal gait (MGI Ref ID J:78134)
- unsteady gait that becomes detectable between 18-21 days of age
- seizures (MGI Ref ID J:78134)
- gently dropping the animals from a height of 10-15cm onto a soft surface frequently induces seizure-like behavior
- tremors (MGI Ref ID J:78134)
- tremors can be consistently induced by a light touch
- hematopoietic system phenotype
- small spleen (MGI Ref ID J:78134)
- thymus atrophy (MGI Ref ID J:78134)
- atrophic thymus
- immune system phenotype
- small spleen (MGI Ref ID J:78134)
- thymus atrophy (MGI Ref ID J:78134)
- atrophic thymus
- vision/eye phenotype
- abnormal eye electrophysiology (MGI Ref ID J:78134)
- electroretinograms have shown abnormal b-waves in three (2 males, 1 female) of four mutants examined
- nervous system phenotype
- seizures (MGI Ref ID J:78134)
- gently dropping the animals from a height of 10-15cm onto a soft surface frequently induces seizure-like behavior
View Research Applications
Research Applications
This mouse can be used to support research in many areas including:Glra1nmf11 related
Endocrine Deficiency Research
Adipose Defects
Internal/Organ Research
Adipose Defects
Spleen Defects
Thymus Defects
Neurobiology Research
Ataxia (Movement) Defects
Epilepsy
Neuroscience Mutagenesis Facility Strain
| Allele Symbol | Glra1nmf11 | ||
|---|---|---|---|
| Allele Name | neuroscience mutagenesis facility, 11 | ||
| Allele Type | Chemically induced (ENU) | ||
| Strain of Origin | C57BL/6J | ||
| 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; | ||
| Molecular Note | This phenotypic mutant was identified in an ENU mutagenesis screen. A cytosine to adenine transition at nucleotide 518 causes a N46K amino acid substitution. A complement test confirmed the gene association. [MGI Ref ID J:112871] [MGI Ref ID J:78134] | ||
This strain will not have a genotyping protocol or one is not currently available.
Helpful Links
Optimizing PCR Protocols
Glra1nmf11 relatedJAX Neuroscience Mutagenesis Facility URL: http://www.jax.org/nmf. 2002. Heritable mouse mutants from JAX NMF ENU Mutagenesis Program MGI Direct Data Submission :. [MGI Ref ID J:78134]
Traka M; Seburn KL; Popko B. 2006. Nmf11 is a novel ENU-induced mutation in the mouse glycine receptor alpha 1 subunit. Mamm Genome 17(9):950-5. [PubMed: 16964444] [MGI Ref ID J:112871]
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 ($)
Weeks of Age Price* Gender Cryorecovery Fee $1900.00
| Pricing for International shipping destinations |
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*Price(s) in US dollars ($)
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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