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EMAGE:3929

Hoxa13 homeobox A13 ( MGI:96173)
TS19 (11.5 dpc)
in situ hybridisation

Data Images
EMAGE:3929
Fig3I(Hoxa13,left,wt). Copyright: Reprinted with permission from Elsevier from [doi:10.1006/dbio.2001.0382] Dev Biol 237: 345-53, Bruneau S; Johnson KR; Yamamoto M; Kuroiwa A; Duboule D, The mouse hoxd13(spdh) mutation, a polyalanine expansion similar to human type ii synpolydactyly (spd), disrupts the function but not the expression of other hoxd genes. Copyright 2001

Expression pattern clarity: three stars
Find spatially similar wholemount expression patterns: Find spatially similar wholemount patterns
Expression Pattern Description
Spatial Annotation:
EMAGE:3929Annotation 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:
3929_wholemount_strong_3D_1.wlz
3929_wholemount_notDetected_3D_1.wlz
(what is wlz format?)
Download all expression domains: EMAGE:3929_all_domains.zip
Find spatially similar wholemount expression patterns:  EMAGE spatially similar wholemount patterns
Morphological match to the template: two stars
Text Annotation:
StructureLevelPatternNotes
limb
detected detected
Annotation Validation: EMAGE Editor
Detection Reagent
Type:in situ hybridisation probe
Identifier:MGI:2153092
Entity Detected:Hoxa13, homeobox A13 ( MGI:96173)
Notes:The Hoxa13 probe used in this study by Bruneau et al., 2001 [PMID:11543619] is described as a gift from F. Rijli. No further information is given to its sequence.
Chemistry:RNA
Strand:antisense
Specimen
Organism:mouse
Age:11.5 dpc
Theiler Stage:TS19
Mutations:none (wild-type)
Preparation:wholemount
Procedures
General Information
Authors:Bruneau S; Johnson KR; Yamamoto M; Kuroiwa A; Duboule D, 2001 [PMID:11543619] , 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:[ doi:10.1006/dbio.2001.0382] [ PMID:11543619] Bruneau S, Johnson KR, Yamamoto M, Kuroiwa A, Duboule D 2001 The mouse Hoxd13(spdh) mutation, a polyalanine expansion similar to human type II synpolydactyly (SPD), disrupts the function but not the expression of other Hoxd genes. Dev Biol (237):345-53
Links:MGI:2153103 same experiment
  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