ASXL3

OMIMHGNC

Synonym(s): KIAA1713

Locus: 18q12.1

Protein: Putative Polycomb group protein ASXL3

 

Disorders

Tests

Test Type
Molecular (6)
Multi-Gene Panel (2)
Multi-Method Panel (3)
Test Method
Del/Dup (CNV) (2)
Sequencing, Capillary (Sanger) (4)
Sequencing, Next Gen (3)
Prenatal/Carrier
Prenatal (2)
Carrier (2)
Lab Location
Portugal(1)
USA(2)
Germany(3)
 
TAT: 8-9 weeks
price: contact lab
Microcephaly Sequencing Panel
method(s): ◦ Sequencing, Next Gen 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 1-3 weeks
price: contact lab
Bainbridge-Ropers Syndrome Test
method(s): ◦ Sequencing, Capillary (Sanger) 
Center for Human Genetics - University of Regensburg, Hehr Laboratory - Regensburg, Germany
Bainbridge-Ropers syndrome (sequence analysis of ASXL3 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 4-5 Weeks
price: contact lab
ASXL3
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
TAT: 3-4 weeks
price: contact lab
Bainbridge-Ropers syndrome
method(s): ◦ Sequencing, Capillary (Sanger) 
Centogene AG, Rare Disease Company - Rostock, Germany
TAT: 4-5 weeks
price: contact lab
Microcephaly panel
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
Centogene AG, Rare Disease Company - Rostock, Germany