Quicksearch Help

(Click the icon to keep this page displayed.)

EMAGE:4357

Cass4 Cas scaffolding protein family member 4 ( MGI:2444482)
TS17 (10.5 dpc)
in situ hybridisation

Data Images
EMAGE:4357
Figure S2. Copyright: This image is from Lu W, PLoS Genet 2007 May 25;3(5):e80 [PMID:17530927] , an open-access article distributed under the terms of the Creative Commons Attribution License.

Expression pattern clarity: one star
Find spatially similar wholemount expression patterns: Find spatially similar wholemount patterns
Notes:
The authors state that there is no expression in the spinal cord.
Expression Pattern Description
Spatial Annotation:
EMAGE:4357Annotation 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:
4357_wholemount_possible_3D_1.wlz
4357_wholemount_notDetected_3D_1.wlz
(what is wlz format?)
Download all expression domains: EMAGE:4357_all_domains.zip
Find spatially similar wholemount expression patterns:  EMAGE spatially similar wholemount patterns
Morphological match to the template: three stars
Text Annotation:
StructureLevelPatternNotes
future spinal cord
not detected not detected
homogeneous
genitourinary system
not detected not detected
homogeneous
Annotation Validation: EMAGE Editor
Detection Reagent
Type:in situ hybridisation probe
Identifier:MGI:3720462
Entity Detected:Cass4, Cas scaffolding protein family member 4 ( MGI:2444482)
Notes:The F730031O20Rik (C20orf32) probe used in this study by Lu et al., 2007 [PMID:17530927] was a "cRNA probe complementary to the 3'-UTR of C20orf32".
Chemistry:RNA
Strand:antisense
Specimen
Organism:mouse
Age:10.5 dpc
Theiler Stage:TS17
Mutations:none (wild-type)
Preparation:wholemount
Procedures
General Information
Authors:Lu W; Quintero-Rivera F; Fan Y; Alkuraya FS; Donovan DJ; Xi Q; Turbe-Doan A; Li QG; Campbell CG; Shanske AL; Sherr EH; Ahmad A; Peters R; Rilliet B; Parvex P; Bassuk AG; Harris DJ; Ferguson H; Kelly C; Walsh CA; Gronostajski RM; Devriendt K; Higgins A; Ligon AH; Quade BJ; Morton CC; Gusella JF; Maas RL, 2007 [PMID:17530927] . 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:10.1371/journal.pgen.0030080] [ PMID:17530927] Lu W, Quintero-Rivera F, Fan Y, Alkuraya FS, Donovan DJ, Xi Q, Turbe-Doan A, Li QG, Campbell CG, Shanske AL, Sherr EH, Ahmad A, Peters R, Rilliet B, Parvex P, Bassuk AG, Harris DJ, Ferguson H, Kelly C, Walsh CA, Gronostajski RM, Devriendt K, Higgins A, Ligon AH, Quade BJ, Morton CC, Gusella JF, Maas RL 2007 NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects. PLoS Genet (3):e80
Links:MGI:3720476 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