Symbol
Name
ID
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Synonyms
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1700022P15Rik, 5830426A08Rik, dyn, neuroaxonal dystrophy, nmf261, ROSA62, SpbIV
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Genetic Map
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Sequence Map
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Mammalian
homology
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Sequences
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All sequences(60)
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Alleles
and
phenotypes
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All alleles(45) :
Targeted, knock-out(2)
Gene trapped(31)
Spontaneous(9)
Chemically induced(3)
| Homozygotes for spontaneous mutations exhibit tremors, progressive ataxia with hind limb paralysis, central deafness, reduced body weight, and shortened lifespan. Males are sterile, but females may breed. |
Phenotype Images (1)
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Polymorphisms
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RFLP(1)
SNPs within 2kb(315 from dbSNP Build 128)
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Gene Ontology
(GO)
classifications
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Expression
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Literature Summary: (3 records)
Data Summary:
Assays (5)
Results (23)
Tissues (17)
Images (4)
Theiler Stages: 10,15,28
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Assay Type |
Assays |
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Results |
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Western blot |
2 |
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6 |
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RT-PCR |
1 |
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1 |
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RNA in situ |
1 |
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4 |
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Northern blot |
1 |
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12 |
cDNA source data(15)
External Resources:
GEO
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Molecular
reagents
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All nucleic(18)
cDNA(17)
Primer pair(1)
Antibodies(1)
Microarray probesets(2)
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Other database
links
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Protein
domains
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References
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(Earliest)
J:167
Yoon CH et al.,
"Quivering, a new first Chromosome mutation in mice"
J Hered 1957;48():176-80
(Latest)
J:142574
Legendre K et al.,
"alphaII-betaV spectrin bridges the plasma membrane and cortical lattice in the lateral wall of the auditory outer hair cells."
J Cell Sci 2008 Oct 15;121(Pt 20):3347-56
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All references(40)
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Other
accession IDs
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MGD-MRK-11840, MGD-MRK-13741, MGD-MRK-9265, MGI:1922798, MGI:1923290, MGI:3514294, MGI:3589010, MGI:97840
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