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EMAGE:891

Lfng LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase ( MGI:1095413)
TS15 (9.5 dpc)
in situ hybridisation

Data Images
EMAGE:891
Fig 6A Dunwoodie et al, 2002 [PMID:11923214] . Copyright: This image is from Development and is displayed with the permission of the Company of Biologists Ltd who owns the copyright.

Expression pattern clarity: three stars
Find spatially similar wholemount expression patterns: Find spatially similar wholemount patterns
Expression Pattern Description
Spatial Annotation:
EMAGE:891Annotation 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:
891_wholemount_strong_3D_1.wlz
891_wholemount_notDetected_3D_1.wlz
(what is wlz format?)
Download all expression domains: EMAGE:891_all_domains.zip
Find spatially similar wholemount expression patterns:  EMAGE spatially similar wholemount patterns
Morphological match to the template: two stars
Text Annotation:
StructureLevelPatternNotes
tail unsegmented mesenchyme
detected detected
regionalTwo domains of expression: rostrally, 1 or 2 bands (the anteriormost just caudal to the forming somite boundary); caudally, extending to the primitive streak
Annotation Validation: EMAGE Editor
Detection Reagent
Type:in situ hybridisation probe
Identifier:MGI:1332541
Entity Detected:Lfng, LFNG O-fucosylpeptide 3-beta-N-acetylglucosaminyltransferase ( MGI:1095413)
Notes:The probe used in this study by Dunwoodie et al, 2002 [PMID:11923214] is described as "Lfng (Johnston et al., 1997 [PMID:9187150] ". Johnston et al do not describe the probe in any detail.
Chemistry:RNA
Strand:antisense
Specimen
Organism:mouse
Strain:129P2/Ola x C57BL/6
Age:9.5 dpc
Theiler Stage:TS15
Mutations:Dll3tm1Rbe/Dll3+
Preparation:wholemount
Procedures
Fixation:Bouin's fixation
General Information
Authors:Dunwoodie et al, 2002 [PMID:11923214] Indexed by GXD, 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:[ PMID:11923214] Dunwoodie SL, Clements M, Sparrow DB, Sa X, Conlon RA, Beddington RS 2002 Axial skeletal defects caused by mutation in the spondylocostal dysplasia/pudgy gene Dll3 are associated with disruption of the segmentation clock within the presomitic mesoderm. Development (129):1795-806
 [ PMID:9187150] Johnston SH, Rauskolb C, Wilson R, Prabhakaran B, Irvine KD, Vogt TF 1997 A family of mammalian Fringe genes implicated in boundary determination and the Notch pathway. Development (124):2245-54
Links:MGI:2178635 same experiment
 MGI:2178443 allele description
  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 SourceMGI