MEG3

OMIMHGNC

Synonym(s): GTL2, NCRNA00023, LINC00023, onco-lncRNA-83

Locus: 14q32.2

Tests

Test Type
Molecular (5)
Multi-Gene Panel (4)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (2)
Methylation Analysis (4)
Uniparental Disomy (1)
Prenatal/Carrier
Carrier (1)
Lab Location
Netherlands(1)
USA(1)
Germany(1)
Canada(1)
Bulgaria(1)
 
TAT: 3-4 weeks
price: contact lab
Congenital Hypotonia Panel: Spinal Muscular Atrophy Deletions, Prader-Willi/Angelman Syndrome Methylation, Myotonic Dystrophy, and Uniparental Disomy 14
method(s):
EGL Genetic Diagnostics, Molecular Genetics Laboratory - Tucker, GA, USA
TAT: 4-8 weeks
price: $330.00
Analysis Methylation status MEG3-DMR for Paternal UPD14 Syndrome (Kagami-Ogata Syndrome) or Maternal UPD14 Syndrome (Temple Syndrome)
method(s): ◦ Methylation Analysis 
Academic Medical Centre, University of Amsterdam, DNA Diagnostics Laboratory - Amsterdam, Netherlands
TAT: 1-3 weeks
price: contact lab
UPD14(mat) like phenotype
method(s): ◦ Del/Dup (CNV) ◦ Methylation Analysis ◦ Uniparental Disomy 
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany
Congenital Hypotonia Panel: Spinal Muscular Atrophy Deletions, Prader-Willi/Angelman Syndrome Methylation, Myotonic Dystrophy, and Uniparental Disomy 14
method(s): ◦ Del/Dup (CNV) ◦ Methylation Analysis 
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada
Uniparental Disomy 14 Test - Malformation syndrome
method(s): ◦ Methylation Analysis 
GMDL Genica - Sofia, Bulgaria