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Familial hemiplegic Migraine (gene panel)

Genetic test Export to PDF
Full name:
Familial hemiplegic Migraine (gene panel)
Description:

core panel: CACNA1A, ATP1A2, SCN1A

full panel: CACNA1A, ATP1A2, SCN1A + ATP1A3, KCNK18, PRRT2, SLC1A3, SLC2A1
Test type:
Clinical
Test specialty:
Molecular Genetics
Test purpose:
Post-natal Diagnosis
Specimen:
Peripheral (whole) blood on EDTA
Method category:
Sequence analysis: entire coding region
Deletion/duplication analysis
Method technique:
Next Generation Sequencing (NGS)
Laboratory:
Centrum Menselijke Erfelijkheid - KUL
RIZIV code:
565493-565504
Turnaround time (maximum):
4 months
Document(s):
Created:
19 Jul 2019 - 10:42
Changed:
15 Oct 2021 - 13:59
URL:
https://laboboeken.nexuzhealth.com/pboek/internet/GHB%20CME/15164
  • Familial hemiplegic Migraine (8 genes) - KUL
    Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments
    CACNA1A 100.00 1 NM001127221.1/ Core gene
    ATP1A2 100.00 1 NM000702.3/ Core gene
    SCN1A 100.00 1 NM_001165963.2/ Core gene
    ATP1A3 100.00 1 NM152296.5/ gene that may be associated with an inherited form of Familia Hemiplegic Migraine (FHM)
    KCNK18 100.00 1 NM181840.1/ gene that may be associated with an inherited form of Familia Hemiplegic Migraine (FHM)
    PRRT2 100.00 1 NM145239.2/ gene that may be associated with an inherited form of Familia Hemiplegic Migraine (FHM)
    SLC1A3 100.00 1 NM004172.4/ gene that may be associated with an inherited form of Familia Hemiplegic Migraine (FHM)
    SLC2A1 100.00 1 NM_006516.2/ gene that may be associated with an inherited form of Familia Hemiplegic Migraine (FHM)