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EMAGE:4633

Abcd2 ATP-binding cassette, sub-family D (ALD), member 2 ( MGI:1349467)
TS17 (11.5 dpc)
in situ hybridisation

Data Images
EMAGE:4633
Fig2A. from [doi:10.1093/hmg/ddi384] Hum Mol Genet 14: 3565-3577, Ferrer I; Kapfhammer JP; Hindelang C; Kemp S; Troffer-Charlier N; Broccoli V; Callyzot N; Mooyer P; Selhorst J; Vreken P; Wanders RJ; Mandel JL; Pujol A, Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage. Copyright 2005

Expression pattern clarity: two stars
Find spatially similar wholemount expression patterns: Find spatially similar wholemount patterns
Expression Pattern Description
Spatial Annotation:
EMAGE:4633Annotation 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:
4633_wholemount_moderate.wlz
4633_wholemount_weak.wlz
4633_wholemount_possible.wlz
4633_wholemount_notDetected.wlz
4633_wholemount_strong.wlz
(what is wlz format?)
Download all expression domains: EMAGE:4633_all_domains.zip
Find spatially similar wholemount expression patterns:  EMAGE spatially similar wholemount patterns
Morphological match to the template: two stars
Text Annotation:
StructureLevelPatternNotes
dorsal root ganglion
strong strong
Annotation Validation: EMAGE Editor
Detection Reagent
Type:in situ hybridisation probe
Identifier:Abcd2 probeA
Entity Detected:Abcd2, ATP-binding cassette, sub-family D (ALD), member 2 ( MGI:1349467)
Notes:The Abcd2 (Aldr) probe used in this study by Ferrer et al., 2005 [PMID:16223892] is described as containing "the C-terminal half of the abcd2 gene, as previously described (Troffer-Charlier et al., 1998 [PMID:9587057] )."
Chemistry:RNA
Strand:antisense
Specimen
Organism:mouse
Age:11.5 dpc
Theiler Stage:TS17
Mutations:none (wild-type)
Preparation:wholemount
Procedures
General Information
Authors:Ferrer I; Kapfhammer JP; Hindelang C; Kemp S; Troffer-Charlier N; Broccoli V; Callyzot N; Mooyer P; Selhorst J; Vreken P; Wanders RJ; Mandel JL; Pujol A, 2005 [PMID:16223892] , 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:10.1093/hmg/ddi384] [ PMID:16223892] Ferrer I, Kapfhammer JP, Hindelang C, Kemp S, Troffer-Charlier N, Broccoli V, Callyzot N, Mooyer P, Selhorst J, Vreken P, Wanders RJ, Mandel JL, Pujol A 2005 Inactivation of the peroxisomal ABCD2 transporter in the mouse leads to late-onset ataxia involving mitochondria, Golgi and endoplasmic reticulum damage. Hum Mol Genet (14):3565-77
 [ doi:10.1016/S0171-9335(98)80121-0] [ PMID:9587057] Troffer-Charlier N, Doerflinger N, Metzger E, Fouquet F, Mandel JL, Aubourg P 1998 Mirror expression of adrenoleukodystrophy and adrenoleukodystrophy related genes in mouse tissues and human cell lines. Eur J Cell Biol (75):254-64
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