Expression Database

GUDMAP:11553
Data Source
   
Gene
Tnfrsf9   tumor necrosis factor receptor superfamily, member 9
   
Theiler Stage TS23
   
   
Images
Development time: 24hrs.
   
Whole-mount in situ hybridization is subject to technical limitations that may influence accuracy of the data (more info).
 
Submitters
Principal Investigator(s): Andrew P McMahon, Harvard University, Cambridge, MA, USA, amcmahon@med.usc.edu
Authors: M Todd Valerius, Andrew P McMahon
Submitted By: M Todd Valerius, Harvard University, Cambridge, MA, USA, tvalerius@mcb.harvard.edu
Archive ID: 173
Submission ID: AM_190309_18
   
Expression Mapping

Expression Strengths Key:
Present (unspecified strength)
Present (strong)
Present (moderate)
Present (weak)
Uncertain
Not Detected
   
Expression Patterns Key:
Homogeneous
Graded
Regional
Spotted
Ubiquitous
Restricted
Single cell
Contains note
View annotated components as a list Show annotation under groups information
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Probe
Gene:
Symbol: Tnfrsf9
Name: tumor necrosis factor receptor superfamily, member 9 (MGI:1101059)
Probe ID: maprobe:5585
Name of cDNA: 5031438N10
Additional Name of cDNA: MSR1659
Sequence ID:
AK019885.1
5' primer sequence: TGGTCATTGTGCTGCTGC
3' primer sequence: TAATACGACTCACTATAGGGATCGGCAGCTACAAGCAT
5' primer location: 123
3' primer location: 825
Origin of Clone used to make the Probe:
Strain: C57BL/6
  Tissue: brain
Probe Type: RNA
Type: antisense
Labelled with: digoxigenin
Visualisation method: alkaline phosphatase + BM purple
Lab Probe ID: 753
Probe Notes: Probe template was amplified from RIKEN clone 5031438N10 using primers designed to the coding region. A T7 promoter sequence was added to the reverse primer for probe transcription. The primers used: Reverse primer sequence = TAATACGACTCACTATAGGGATCGGCAGCTACAAGCAT : Forward primer sequence= TGGTCATTGTGCTGCTGC. MSR1659.
   
Specimen
Theiler Stage: TS23
Other Staging System: 15.5dpc
Tissue:
Strain: Swiss Webster
Genotype: Wild type
Sex: female
Specimen Preparation:
wholemount
Fixation Method: 4% paraformaldehyde
  
Linked Publications
   
Linked Submissions
   
Acknowledgements
Jinjin Guo, Mary Duah, Joe Vaughan & Diane Faria are acknowledged for their technical assistance on the GUDMAP project. JV & DF performed mouse dissection. MD was responsible for clone procurement. JG & MD performed template PCR reactions and performed hybridizations. MT Valerius designed the probes, annotated the expression patterns and managed the data.

 

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Department of Health and Human Services National Institutes of Health Contacts Citing GUDMAP National Institute of Diabetes and National Institute of Child Health and Human Development