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EMAGE:5005

Dmd dystrophin, muscular dystrophy ( MGI:94909)
TS15 (9.5 dpc)
in situ hybridisation

Data Images
EMAGE:5005
Fig4Y. Copyright: This image is from [doi:10.1002/(SICI)1097-0177(199806)212:2<229::AID-AJA7>3.0.CO;2-J] Wertz K; Fuchtbauer EM, " Dmd(mdx-beta geo): a new allele for the mouse dystrophin gene." Dev Dyn 1998 Jun;212(2):229-41. Reprinted with permission of Wiley-Liss Inc. [PMID:9626497] .

Expression pattern clarity: two stars
Find spatially similar wholemount expression patterns: Find spatially similar wholemount patterns
Expression Pattern Description
Spatial Annotation:
EMAGE:5005Annotation colour key:  
strong strong      
gene expression moderate moderate    
gene expression weak weak        
gene expression possible possible    
gene expression not detected not detected
wholemount mapping

Download individual expression domains:
5005_wholemount_moderate.wlz
5005_wholemount_notDetected.wlz
5005_wholemount_strong.wlz
5005_wholemount_possible.wlz
(what is wlz format?)
Download all expression domains: EMAGE:5005_all_domains.zip
Find spatially similar wholemount expression patterns:  EMAGE spatially similar wholemount patterns
Morphological match to the template: three stars
Text Annotation:
StructureLevelPatternNotes
trunk somite
detected detected
gradedexpression is found in the lateral somite, with greater staining in the posterior part of each segment.
forelimb bud mesenchyme
detected detected
regionalstained cells are found scattered in the dorsal mesenchyme of the limb buds.
hindlimb ridge mesenchyme
detected detected
regionalstained cells are found scattered in the dorsal mesenchyme of the limb buds.
heart
weak weak
regionalgene starts to be expressed weakly in the region around the developing atrioventricular valves.
future hindbrain
detected detected
regionalexpression is found in the roof of the rhombencephalon, in the optic vesicle, and in the floor plate.
optic vesicle
detected detected
telencephalon
strong strong
Annotation Validation: EMAGE Editor
Detection Reagent
Type:in situ hybridisation probe
Identifier:Dmd probeA
Entity Detected:Dmd, dystrophin, muscular dystrophy ( MGI:94909)
Notes:The Dmd probe used in this study by Wertz and Fuchtbauer, 1998 [PMID:9626497] recognises dystrophin exons 66-75, yet it is of unreported sequence.
Chemistry:RNA
Strand:antisense
Specimen
Organism:mouse
Age:9.5 dpc
Theiler Stage:TS15
Mutations:none (wild-type)
Preparation:wholemount
Procedures
General Information
Authors:Wertz K and Fuchtbauer EM, 1998 [PMID:9626497] , Indexed and Spatially Mapped by EMAGE.
Submitted by:EMAGE EDITOR, Institute of Genetics and Molecular Medicine, Western General Hospital, Crewe Road, Edinburgh, UK EH4 2XU
Experiment type:non-screen
References:[ doi:10.1002/(SICI)1097-0177(199806)212:2<229::AID-AJA7>3.0.CO;2-J] [ PMID:9626497] Wertz K, Fuechtbauer EM 1998 Dmd(mdx-beta geo): a new allele for the mouse dystrophin gene. Dev Dyn (1998):229-41
Links: Ensembl same gene
  Allen Brain Atlas same gene
  BioGPS same gene
  International Mouse Knockout Project Status same gene
  GEISHA Chicken ISH Database same gene
  EMBL-EBI Gene Expression Atlas same gene
  BrainStars same gene
  ViBrism same gene
Data SourceEMAGE