Quicksearch Help

(Click the icon to keep this page displayed.)

EMAGE:5920

Cd96 CD96 antigen ( MGI:1934368)
TS15 (10.0 dpc)
in situ hybridisation

Data Images
EMAGE:5920
Figure 2B. [doi:10.1086/522014] Kaname T; Yanagi K; Chinen Y; Makita Y; Okamoto N; Maehara H; Owan I; Kanaya F; Kubota Y; Oike Y; Yamamoto T; Kurosawa K; Fukushima Y; Bohring A; Opitz JM; Yoshiura K; Niikawa N; Naritomi K, "Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome." Am J Hum Genet 2007; 81: 835-41. [PMID:17847009]

Expression pattern clarity: two stars
Find spatially similar wholemount expression patterns: Find spatially similar wholemount patterns
Expression Pattern Description
Spatial Annotation:
EMAGE:5920Annotation 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:
5920_wholemount__moderate.wlz
5920_wholemount__possible.wlz
5920_wholemount__notDetected.wlz
5920_wholemount__strong.wlz
(what is wlz format?)
Download all expression domains: EMAGE:5920_all_domains.zip
Find spatially similar wholemount expression patterns:  EMAGE spatially similar wholemount patterns
Morphological match to the template: two stars
Text Annotation:
StructureLevelPatternNotes
blood
detected detected
future forebrain
detected detected
pharynx
detected detected
embryo
detected detected
regionalExpression is in front part of the head
heart
detected detected
Expression in cardiac jelly.
Annotation Validation: Submitter + EMAGE Editor
Detection Reagent
Type:in situ hybridisation probe
Identifier:MGI:3807076
Entity Detected:Cd96, CD96 antigen ( MGI:1934368)
Notes:The Cd96 probe used in this study by Kaname et al., 2007 [PMID:17847009] is of unreported sequence.
Chemistry:RNA
Strand:antisense
Specimen
Organism:mouse
Age:10.0 dpc
Theiler Stage:TS15
Mutations:none (wild-type)
Preparation:wholemount
Procedures
General Information
Authors:Kaname T; Yanagi K; Chinen Y; Makita Y; Okamoto N; Maehara H; Owan I; Kanaya F; Kubota Y; Oike Y; Yamamoto T; Kurosawa K; Fukushima Y; Bohring A; Opitz JM; Yoshiura K; Niikawa N; Naritomi K, 2007 [PMID:17847009] . 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:10.1086/522014] [ PMID:17847009] Kaname T, Yanagi K, Chinen Y, Makita Y, Okamoto N, Maehara H, Owan I, Kanaya F, Kubota Y, Oike Y, Yamamoto T, Kurosawa K, Fukushima Y, Bohring A, Opitz JM, Yoshiura K, Niikawa N, Naritomi K 2007 Mutations in CD96, a member of the immunoglobulin superfamily, cause a form of the C (Opitz trigonocephaly) syndrome. Am J Hum Genet (81):835-41
Links:MGI:3807077 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