In collaboration with Prof. Dr. Thomas Gasser, University of Tübingen, Germany, CeGaT has developed a Parkinson Panel for simultaneously analyzing all known genes associated with Parkinson.
The sequencing of the genes mentioned below is performed on the SOLiD platforms via next generation sequencing. The obtained data are analyzed based on the particular request. All variants being found are validated on the capillary sequencer.
For diagnostic purposes and based on the particular phenotype the whole Parkinson Panel (consisting of the four sub-panels) or each of the below described sub-panels can be ordered. The price depends on the number of genes ordered and will be gladly provided upon request. A deletion analysis can be requested separately.
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Sub-Panel 1: Parkinson Syndrome (autosomal dominant):
- LRRK2
- SNCA
- GBA
- VPS35A
Sub-Panel 2: Parkinson Syndrome (autosomal recessive):
- PARKIN
- PINK1
- DJ1
Sub-Panel 3: Atypical Parkinson Syndrome:
- ATP13A2
- DCTN1
- POLG
- ATP1A3
- GCH1
- TH
- PLA2G6
- MAPT
- FBX07
- CSF1R
Sub-Panel 4: Parkinson-Dystonia Syndrome:
- TAF1
- SLC6A3 (infantile)
- ATP1A3
- PRKRA (DYT16)
- PLA2G6
We also do gene testing of single genes - please send a request at info {at} cegat.de. Further information can be found in the section Molecular Diagnostics.
