PIGW

OMIMHGNC

Synonym(s): Gwt1, FLJ37433

Locus: 17q12

Protein: Phosphatidylinositol-glycan biosynthesis class W protein

 

Disorders

Tests

Test Type
Molecular (4)
Multi-Gene Panel (2)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (2)
Sequencing, Capillary (Sanger) (2)
Sequencing, Next Gen (3)
Prenatal/Carrier
Prenatal (1)
Carrier (2)
Lab Location
USA(1)
Canada(1)
Germany(2)
 
TAT: 4-5 Weeks
price: contact lab
PIGW
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Mabry Syndrome: Sequencing Panel
method(s): ◦ Sequencing, Next Gen 
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada
TAT: 3-4 weeks
price: contact lab
Hyperphosphatasia with mental retardation syndrome type 5
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany
TAT: 4-6 weeks
price: contact lab
GPI anchor deficiency with or without Hyperphosphatasia (12 Genes, EPI12)
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany