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Search results 1 to 100 out of 416 for Dst

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Type Details Score
Gene
667 | DST
Type: gene
Organism: human
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Gene
100333215 | dst
Type: gene
Organism: zebrafish
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Gene
100430705 | DST
Type: gene
Organism: macaque, rhesus
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Gene
100496778 | dst
Type: gene
Organism: frog, western clawed
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Gene
316313 | Dst
Type: gene
Organism: rat
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Gene
462793 | DST
Type: gene
Organism: chimpanzee
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Gene
474948 | DST
Type: gene
Organism: dog, domestic
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Gene
535297 | DST
Type: gene
Organism: cattle
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Gene
421884 | DST
Type: gene
Organism: chicken
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Protein Coding Gene
MGI:104627 | Dst
Type: protein_coding_gene
Organism: mouse, laboratory
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Gene
101930010 | DST-AS1
Type: gene
Organism: human
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Publication
- | J:115254
     
First Author: Harris B
Year: 2006
Journal: MGI Direct Data Submission
Title: Dst35J, a remutation of Dst
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GXD Expression
GXD Expression
   
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1689419
Pattern: Not Specified
Stage: TS19
Assay Id: MGI:6190154
Age: embryonic day 11.5
Specimen Label: Table S2 - E11.5 - Dst
Detected: true
Specimen Num: 1
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GXD Expression
GXD Expression
   
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Not Specified
Emaps: EMAPS:1689421
Pattern: Not Specified
Stage: TS21
Assay Id: MGI:6190154
Age: embryonic day 13.5
Specimen Label: Table S2 - E13.5 - Dst
Detected: true
Specimen Num: 2
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GXD Expression
GXD Expression
   
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689424
Pattern: Not Specified
Stage: TS24
Assay Id: MGI:6190154
Age: embryonic day 15.5
Specimen Label: Table S2 - E15.5 - Dst
Detected: true
Specimen Num: 3
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GXD Expression
GXD Expression
   
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689426
Pattern: Not Specified
Stage: TS26
Assay Id: MGI:6190154
Age: embryonic day 18.5
Specimen Label: Table S2 - E18.5 - Dst
Detected: true
Specimen Num: 4
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GXD Expression
GXD Expression
   
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689428
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6190154
Age: postnatal day 4
Specimen Label: Table S2 - P4 - Dst
Detected: true
Specimen Num: 5
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GXD Expression
GXD Expression
   
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689428
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6190154
Age: postnatal day 14
Specimen Label: Table S2 - P14 - Dst
Detected: true
Specimen Num: 6
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GXD Expression
GXD Expression
   
Probe: MGI:6171520
Assay Type: RNA in situ
Annotation Date: 2018-07-25
Strength: Present
Sex: Male
Emaps: EMAPS:1689428
Pattern: Not Specified
Stage: TS28
Assay Id: MGI:6190154
Age: postnatal day 28
Specimen Label: Table S2 - P28 - Dst
Detected: true
Specimen Num: 7
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Publication
32482619 | J:291060
 
First Author: Yoshioka N
Year: 2020
Journal: Dis Model Mech
Title: Diverse dystonin gene mutations cause distinct patterns of Dst isoform deficiency and phenotypic heterogeneity in Dystonia musculorum mice.
Volume: 13
Issue: 5
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Publication
- | J:157224
     
First Author: Dionne L
Year: 2010
Journal: Personal Communication
Title: Dystonia musculorum 39 Jackson
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Publication
- | J:155854
     
First Author: Harris BS
Year: 1998
Journal: Personal Communication, The Jackson Laboratory
Title: Documentation of phenotype for allele Dstdt-31J
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Publication
- | J:155853
     
First Author: Harris BS
Year: 1998
Journal: Personal Communication, The Jackson Laboratory
Title: Documentation of information for allele Dstdt-30J
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Publication
25195653 | J:228781
First Author: Horie M
Year: 2014
Journal: Eur J Neurosci
Title: Disruption of actin-binding domain-containing Dystonin protein causes dystonia musculorum in mice.
Volume: 40
Issue: 10
Pages: 3458-71
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Publication
28664402 | J:262097
First Author: Hossain MI
Year: 2018
Journal: Neurochem Res
Title: Reduced Proliferation of Oligodendrocyte Progenitor Cells in the Postnatal Brain of Dystonia Musculorum Mice.
Volume: 43
Issue: 1
Pages: 92-100
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Publication
27693510 | J:251779
 
First Author: Horie M
Year: 2016
Journal: Neurobiol Dis
Title: Characterization of novel dystonia musculorum mutant mice: Implications for central nervous system abnormality.
Volume: 96
Pages: 271-283
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Author
Ong DST
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Publication
32445516 | J:297568
First Author: Horie M
Year: 2020
Journal: Glia
Title: Disruption of dystonin in Schwann cells results in late-onset neuropathy and sensory ataxia.
Volume: 68
Issue: 11
Pages: 2330-2344
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Protein
Q80VL5
Organism: Mus musculus/domesticus
Length: 232  
Fragment?: true
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Protein
A3KMF5
Organism: Mus musculus/domesticus
Length: 267  
Fragment?: true
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Publication
35942699 | J:332330
   
First Author: Yoshioka N
Year: 2022
Journal: Elife
Title: Isoform-specific mutation in Dystonin-b gene causes late-onset protein aggregate myopathy and cardiomyopathy.
Volume: 11
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Publication
- | J:218962
     
First Author: SoRelle J
Year: 2015
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for tinsel
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Publication
29061384 | J:260687
     
First Author: Hossain MI
Year: 2017
Journal: Neurochem Int
Title: Motoneuron degeneration in the trigeminal motor nucleus innervating the masseter muscle in Dystonia musculorum mice.
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Publication
- | J:94340
     
First Author: The Jackson Laboratory Office of Genetic Resources
Year: 2000
Journal: MGI Direct Data Submission
Title: Registry of Remutation at The Jackson Laboratory
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Publication
9581287 | J:47356
First Author: Bernier G
Year: 1998
Journal: Dev Genet
Title: Prenatal onset of axonopathy in Dystonia musculorum mice.
Volume: 22
Issue: 2
Pages: 160-8
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Publication
24381311 | J:209161
First Author: Ferrier A
Year: 2014
Journal: Hum Mol Genet
Title: Transgenic expression of neuronal dystonin isoform 2 partially rescues the disease phenotype of the dystonia musculorum mouse model of hereditary sensory autonomic neuropathy VI.
Volume: 23
Issue: 10
Pages: 2694-710
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Publication
8954775 | J:36985
First Author: Bernier G
Year: 1996
Journal: Genomics
Title: Cloning and characterization of mouse ACF7, a novel member of the dystonin subfamily of actin binding proteins.
Volume: 38
Issue: 1
Pages: 19-29
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Protein Coding Gene
MGP_CAROLIEiJ_G0014019 | -
Type: protein_coding_gene
Organism: Mus caroli
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Protein Coding Gene
MGP_129S1SvImJ_G0015906 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AJ_G0015890 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_AKRJ_G0015846 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_BALBcJ_G0015844 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C3HHeJ_G0015678 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGI_C57BL6J_104627 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_C57BL6NJ_G0016297 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CASTEiJ_G0015258 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_CBAJ_G0015649 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_DBA2J_G0015750 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_FVBNJ_G0015752 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_LPJ_G0015820 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NODShiLtJ_G0015772 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_NZOHlLtJ_G0016344 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PWKPhJ_G0015041 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_WSBEiJ_G0015320 | -
Type: protein_coding_gene
Organism: mouse, laboratory
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Protein Coding Gene
MGP_PahariEiJ_G0027265 | -
Type: protein_coding_gene
Organism: Mus pahari
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Protein Coding Gene
MGP_SPRETEiJ_G0014824 | -
Type: protein_coding_gene
Organism: Mus spretus
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Publication
10357897 | J:55704
First Author: Dalpé G
Year: 1999
Journal: Dev Biol
Title: Dystonin-deficient mice exhibit an intrinsic muscle weakness and an instability of skeletal muscle cytoarchitecture.
Volume: 210
Issue: 2
Pages: 367-80
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Publication
11514586 | J:80762
First Author: Leung CL
Year: 2001
Journal: J Cell Biol
Title: The BPAG1 locus: Alternative splicing produces multiple isoforms with distinct cytoskeletal linker domains, including predominant isoforms in neurons and muscles.
Volume: 154
Issue: 4
Pages: 691-7
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Publication
16289082 | J:104464
First Author: Young KG
Year: 2006
Journal: Exp Cell Res
Title: A Bpag1 isoform involved in cytoskeletal organization surrounding the nucleus.
Volume: 312
Issue: 2
Pages: 121-34
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Publication
7736575 | J:24974
First Author: Guo L
Year: 1995
Journal: Cell
Title: Gene targeting of BPAG1: abnormalities in mechanical strength and cell migration in stratified epithelia and neurologic degeneration.
Volume: 81
Issue: 2
Pages: 233-43
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Publication
8752219 | J:35022
First Author: Yang Y
Year: 1996
Journal: Cell
Title: An essential cytoskeletal linker protein connecting actin microfilaments to intermediate filaments.
Volume: 86
Issue: 4
Pages: 655-65
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Publication
20209123 | J:158696
First Author: Boyer JG
Year: 2010
Journal: PLoS One
Title: Hearts of dystonia musculorum mice display normal morphological and histological features but show signs of cardiac stress.
Volume: 5
Issue: 3
Pages: e9465
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Publication
9468135 | J:91502
First Author: Eyer J
Year: 1998
Journal: Nature
Title: Pathogenesis of two axonopathies does not require axonal neurofilaments.
Volume: 391
Issue: 6667
Pages: 584-7
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Publication
- | J:61053
     
First Author: Harris BS
Year: 2000
Journal: MGI Direct Data Submission
Title: The Jackson Laboratory Mouse Mutant Resource 2000 Mutation Reports
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Publication
16341670 | J:104061
First Author: Pool M
Year: 2005
Journal: Mamm Genome
Title: Genetic alterations at the Bpag1 locus in dt mice and their impact on transcript expression.
Volume: 16
Issue: 12
Pages: 909-17
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Publication
9570777 | J:48174
First Author: Bernier G
Year: 1998
Journal: Development
Title: Dystonin is an essential component of the Schwann cell cytoskeleton at the time of myelination.
Volume: 125
Issue: 11
Pages: 2135-48
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Publication
9618216 | J:91495
First Author: Dalpé G
Year: 1998
Journal: Mol Cell Neurosci
Title: Dystonin Is Essential for Maintaining Neuronal Cytoskeleton Organization.
Volume: 10
Issue: 5/6
Pages: 243-57
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Publication
8742268 | J:31811
First Author: Bernier G
Year: 1995
Journal: Mol Cell Neurosci
Title: Dystonin expression in the developing nervous system predominates in the neurons that degenerate in dystonia musculorum mutant mice.
Volume: 6
Issue: 6
Pages: 509-20
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Publication
8714679 | J:31305
First Author: Bernier G
Year: 1995
Journal: Biochem Cell Biol
Title: Dystonin transcripts are altered and their levels are reduced in the mouse neurological mutant dt24J.
Volume: 73
Issue: 9-10
Pages: 605-9
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Publication
- | J:218968
     
First Author: Reyna C
Year: 2015
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for phelps
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Publication
12859670 | J:91505
First Author: De Repentigny Y
Year: 2003
Journal: J Neurochem
Title: Impaired fast axonal transport in neurons of the sciatic nerves from dystonia musculorum mice.
Volume: 86
Issue: 3
Pages: 564-71
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Publication
26886550 | J:249278
First Author: Kornfeld SF
Year: 2016
Journal: PLoS One
Title: Cytoskeletal Linker Protein Dystonin Is Not Critical to Terminal Oligodendrocyte Differentiation or CNS Myelination.
Volume: 11
Issue: 2
Pages: e0149201
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Publication
21698255 | J:174783
First Author: De Repentigny Y
Year: 2011
Journal: PLoS One
Title: Motor unit abnormalities in Dystonia musculorum mice.
Volume: 6
Issue: 6
Pages: e21093
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Publication
- | J:27517
 
First Author: Sweet HO
Year: 1994
Journal: Mouse Genome
Title: Remutation - dt27J
Volume: 92
Pages: 672
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Publication
22190742 | J:197011
First Author: Ryan SD
Year: 2012
Journal: Mol Biol Cell
Title: Neuronal dystonin isoform 2 is a mediator of endoplasmic reticulum structure and function.
Volume: 23
Issue: 4
Pages: 553-66
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Publication
29982604 | J:266479
First Author: Lynch-Godrei A
Year: 2018
Journal: Hum Mol Genet
Title: Dystonin-A3 upregulation is responsible for maintenance of tubulin acetylation in a less severe dystonia musculorum mouse model for hereditary sensory and autonomic neuropathy type VI.
Volume: 27
Issue: 20
Pages: 3598-3611
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Publication
14188280 | J:15323
 
First Author: DUCHEN LW
Year: 1964
Journal: Brain
Title: CLINICAL AND PATHOLOGICAL STUDIES OF AN HEREDITARY NEUROPATHY IN MICE (DYSTONIA MUSCULORUM).
Volume: 87
Pages: 367-78
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Publication
133598 | J:5674
 
First Author: Duchen LW
Year: 1976
Journal: Adv Neurol
Title: Dystonia musculorum--an inherited disease of the nervous system in the mouse.
Volume: 14
Pages: 353-65
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Publication
4655279 | J:5330
First Author: Janota I
Year: 1972
Journal: Brain
Title: Ultrastructural studies of an hereditary sensory neuropathy in mice (dystonia musculorum).
Volume: 95
Issue: 3
Pages: 529-36
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Publication
10381265 | J:57360
First Author: Hartmann N
Year: 1999
Journal: J Cell Biochem
Title: Dystonia musculorum mutation and myosin heavy chain expression in skeletal and cardiac muscles.
Volume: 74
Issue: 1
Pages: 90-8
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Publication
1389184 | J:2788
First Author: Campbell RM
Year: 1992
Journal: Neuron
Title: An intrinsic neuronal defect operates in dystonia musculorum: a study of dt/dt<==>+/+ chimeras.
Volume: 9
Issue: 4
Pages: 693-703
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Publication
7217981 | J:6491
First Author: Moss TH
Year: 1981
Journal: J Neurol Sci
Title: Schwann cell involvement in the neurological lesion of the dystonic mutant mouse. A nerve grafting study.
Volume: 49
Issue: 2
Pages: 207-22
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Publication
- | J:64095
 
First Author: Falconer DS
Year: 1961
Journal: Mouse News Lett
Title: Mutation Dstdt dystonia musculorum
Volume: 25
Pages: 30
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Publication
- | J:15350
 
First Author: Hanker JS
Year: 1976
Journal: Neuropathol Appl Neurobiol
Title: Histochemical and ultrastructural studies on primary sensory neurons in mice with dystonia musculorum. I. Acetylcholinesterase and lysosomal hydrolases.
Volume: 2
Pages: 79-97
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Publication
10842346 | J:113185
First Author: Ongali B
Year: 2000
Journal: Synapse
Title: Dopamine D(1) and D(2) receptors in the forebrain of dystonia musculorum mutant mice: an autoradiographic survey in relation to dopamine contents.
Volume: 37
Issue: 1
Pages: 1-15
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Publication
- | J:160
 
First Author: Falconer DS
Year: 1964
Journal: Mouse News Lett
Title: Allelism of athetoid (ah) and dystonia (dt)
Volume: 31
Pages: 21
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Publication
11841918 | J:91450
First Author: Strazielle C
Year: 2002
Journal: J Chem Neuroanat
Title: Biochemical and autoradiographic studies of the central noradrenergic system in dystonia musculorum mutant mice.
Volume: 23
Issue: 2
Pages: 143-55
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Publication
3138544 | J:17844
First Author: Kothary R
Year: 1988
Journal: Nature
Title: A transgene containing lacZ inserted into the dystonia locus is expressed in neural tube.
Volume: 335
Issue: 6189
Pages: 435-7
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Publication
16087202 | J:106403
First Author: Lalonde R
Year: 2005
Journal: Physiol Behav
Title: Primary neurologic screening and motor coordination of Dstdt-J mutant mice (dystonia musculorum) with spinocerebellar atrophy.
Volume: 86
Issue: 1-2
Pages: 46-51
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Publication
7938238 | J:19530
First Author: Lalonde R
Year: 1994
Journal: Physiol Behav
Title: Exploration and motor coordination in dystonia musculorum mutant mice.
Volume: 56
Issue: 2
Pages: 277-80
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Publication
8327590 | J:16000
First Author: Lalonde R
Year: 1993
Journal: Physiol Behav
Title: Swimming activity in dystonia musculorum mutant mice.
Volume: 54
Issue: 1
Pages: 119-20
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Publication
- | J:37368
 
First Author: Lane PW
Year: 1958
Journal: Mouse News Lett
Title: Athetoid - ah
Volume: 19
Pages: 25
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Publication
542100 | J:6300
First Author: Messer A
Year: 1979
Journal: Life Sci
Title: Changes in whole tissue biosynthesis of gamma-amino butyric acid (GABA) in basal ganglia of the dystonia (dtAlb) mouse.
Volume: 25
Issue: 26
Pages: 2217-21
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Publication
6115889 | J:6585
First Author: Riker DK
Year: 1981
Journal: J Neurochem
Title: Increased noradrenergic metabolism in the cerebellum of the mouse mutant dystonia musculorum.
Volume: 37
Issue: 3
Pages: 649-54
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Publication
- | J:64441
 
First Author: Messer A
Year: 1978
Journal: Mouse News Lett
Title: Dstdt-alb - dystonia musculorum-Albany
Volume: 59
Pages: 39
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Publication
16725123 | J:120587
 
First Author: Goryunov D
Year: 2007
Journal: Brain Res
Title: Molecular characterization of the genetic lesion in Dystonia musculorum (dt-Alb) mice.
Volume: 1140
Pages: 179-87
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Publication
7374955 | J:6316
First Author: Messer A
Year: 1980
Journal: Neuroscience
Title: An allele of the mouse mutant dystonia musculorum exhibits lesions in red nucleus and striatum.
Volume: 5
Issue: 3
Pages: 543-9
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Publication
- | J:218961
     
First Author: SoRelle J
Year: 2015
Journal: MGI Direct Data Submission
Title: Mutagenetix entry for gobble
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Publication
16289886 | J:104592
First Author: Ichikawa H
Year: 2006
Journal: Neuroscience
Title: The survival of vagal and glossopharyngeal sensory neurons is dependent upon dystonin.
Volume: 137
Issue: 2
Pages: 531-6
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Publication
18619576 | J:139985
 
First Author: Ichikawa H
Year: 2008
Journal: Brain Res
Title: The number of nociceptors in the trigeminal ganglion but not proprioceptors in the mesencephalic trigeminal tract nucleus is reduced in dystonin deficient dystonia musculorum mice.
Volume: 1226
Pages: 33-8
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MouseMine is a collaboration between MGI at The Jackson Laboratory and the InterMine project at the Cambridge Systems Biology Centre. MouseMine is funded through a grant from the NIH/NHGRI.The Jackson Laboratory makes no representation about the suitability or accuracy of this software or data for any purpose, and makes no warranties, either express or implied, including merchantability and fitness for a particular purpose or that the use of this software or data will not infringe any third party patents, copyrights, trademarks, or other rights. the software and data are provided "as is". This software and data are provided to enhance knowledge and encourage progress in the scientific community and are to be used only for research and educational purposes. Any reproduction or use for commercial purpose is prohibited without the prior express written permission of the Jackson Laboratory.

Copyright © 2017 by The Jackson Laboratory. All Rights Reserved

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