HuDSeN:374

FRMD7 FERM domain containing 7(NM_194277)
CS CS22
in situ hybridisation

Data Images
HuDSeN:374 HuDSeN:374
Expression pattern clarity: two stars
Find spatially similar expression patterns: Find spatially similar patterns
Detection Reagent
Type:in situ hybridisation probe
Identifier:NYS1
Entity Detected:FRMD7, FERM domain containing 7(NM_194277)
Sequence:nt 1064 - nt 1700 of NM_194277
Probe generated from:cDNA
Chemistry:RNA
Strand:antisense
Label:digoxigenin
Specimen
Organism:human
Carnegie Stage:CS22
Preparation:section
Expression Pattern Description
Text Annotation:
StructureLevelPatternNotes
hindbrain
strong strong
not applicable
telencephalon
strong strong
not applicable
hypothalamus
strong strong
not applicable
midbrain
strong strong
not applicable
Spatial Annotation:
HuDSeN:374HuDSeN:374HuDSeN:374
3D mapping3D mappingspatial mapping

Annotation colour key:   strong strong       moderate moderate     weak weak         possible possible     not detected not detected
Find spatially similar expression patterns: Find spatially similar patterns
Morphological match to the template: two stars
Spatial mapping approved by: EADHB Editor
Procedures
Fixation:4% paraformaldehyde
Staining procedure:alkaline phosphatase + NBT/BCIP
General Information
Principal investigator:Dr Lucy Raymond, University of Cambridge, Cambridge Institute of Medical Research, Wellcome/MRC Building, Cambridge, UK CB2 2XY
Submitted by:Janet Kerwin, Institute of Human Genetics, Newcastle University, International Centre for Life, Central Parkway, Newcastle upon Tyne, UK NE1 3BZ
Experiment type:non-screen
References:PMID: 17013395 Tarpey P, Thomas S, Sarvananthan N, Mallya U, Lisgo S, Talbot CJ, Roberts EO, Awan M, Surendran M, McLean RJ, Reinecke RD, Langmann A, Lindner S, Koch M, Jain S, Woodruff G, Gale RP, Degg C, Droutsas K, Asproudis I, Zubcov AA, Pieh C, Veal CD, Machado RD, Backhouse OC, Baumber L, Constantinescu CS, Brodsky MC, Hunter DG, Hertle RW, Read RJ, Edkins S, O'Meara S, Parker A, Stevens C, Teague J, Wooster R, Futreal PA, Trembath RC, Stratton MR, Raymond FL, Gottlob I. 2006 Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmus Nat Genet (38):1242-4
Acknowledgments:The human embryonic material was provided by the Joint MRC-Wellcome Trust Human Developmental Biology Resource (http://www.hdbr.org) at the IHG, Newcastle-upon-Tyne, UK
Links: EMAGE same gene
  Allen Brain Atlas same gene
  BioGPS same gene

Entries are submitted to the HuDSeN database using the official gene name, according to the HUGO Gene Nomenclature Committee, at the time of uploading. If an official gene name subsequently changes after submission of the entry to the database, the previous name may be shown in the table above.


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