PGAP3

OMIMHGNC

Synonym(s): MGC9753, CAB2, PP1498, PER1, PERLD1

Locus: 17q21.2

Protein: Post-GPI attachment to proteins factor 3

 

Disorders

Tests

Test Type
Molecular (5)
Multi-Gene Panel (4)
Multi-Method Panel (1)
Test Method
Del/Dup (CNV) (3)
Sequencing, Capillary (Sanger) (1)
Sequencing, Next Gen (4)
Prenatal/Carrier
Prenatal (1)
Carrier (2)
Lab Location
USA(3)
Canada(1)
Germany(1)
 
TAT: 8-10 weeks
price: contact lab
Epilepsy Exome Panel
method(s): ◦ Sequencing, Next Gen 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 2-4 weeks
price: contact lab
Comprehensive Epilepsy (NextGen Sequencing Panel and Copy Number Analysis; 502 genes + mtDNA)
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA
TAT: 2-4 weeks
price: contact lab
Myoclonic Epilepsy (NextGen Sequencing Panel and Copy Number Analysis; 93 Genes)
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
MNG Laboratories (Medical Neurogenetics, LLC.) - Atlanta, GA, USA
Mabry Syndrome: Sequencing Panel
method(s): ◦ Sequencing, Next Gen 
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada
TAT: ~2 weeks
price: contact lab
Hyperphosphatasia with mental retardation syndrome type 4
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany