Expression Database

Data Source
   
Gene
Porcn   porcupine homolog (Drosophila)
   
Theiler Stage TS23
   
   
Images
Weak, ubiquitous signal. 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: 125
Submission ID: 20080630-41
   
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
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Probe
Gene:
Symbol: Porcn
Name: porcupine homolog (Drosophila) (MGI:1890212)
Probe ID: maprobe:5197
Name of cDNA: 2410004O13
Sequence ID:
AK010405.1
5' primer sequence: GCTGGTGAGATGCACATG
3' primer sequence: TAATACGACTCACTATAGGGCGGTAGAAGATCCAGCAT
5' primer location: 283
3' primer location: 985
Origin of Clone used to make the Probe:
cDNA Strain: C57BL/6
  Tissue: brain
Probe Type: RNA
Type: antisense
Labelled with: digoxigenin
Visualisation method: alkaline phosphatase + BM purple
Probe Notes: Probe template was amplified from RIKEN clone 2410004O13 using primers designed to the coding region (when annotated). A T7 promoter sequence was added to the reverse primer for probe transcription. The primers used: Reverse primer sequence = TAATACGACTCACTATAGGGCGGTAGAAGATCCAGCAT : Forward primer sequence= GCTGGTGAGATGCACATG
   
Specimen
Theiler Stage: TS23
Other Staging System: 15.5dpc
Tissue:
Strain: Swiss Webster
Genotype: Wild type
Sex: male
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 performed template PCR reactions. MT Valerius produced the probes, performed hybridizations, 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