DPY19L2

OMIMHGNC

Synonym(s): FLJ32949, SPATA34

Locus: 12q14.2

Protein: Probable C-mannosyltransferase DPY19L2

 

Disorders

Tests

Test Type
Molecular (6)
Multi-Gene Panel (2)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (2)
Sequencing, Capillary (Sanger) (3)
Sequencing, Next Gen (4)
Prenatal/Carrier
Carrier (3)
Lab Location
Portugal(1)
Spain(2)
USA(1)
Austria(1)
Germany(1)
 
Spermatogenic failure 9 (SPGF9, sequence analysis of DPY19L2 gene)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal
Male Infertility due to Globozoospermia, Sequencing DPY19L2
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 4-5 Weeks
price: contact lab
DPY19L2
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Spermatogenic failure (Spermatogenese-Defekt)
method(s): ◦ Sequencing, Next Gen 
Praxis fuer Humangenetik Wien - Vienna, Austria
Spermatogenic Failure, Panel Massive Sequencing (NGS) 9 Genes
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: ~2 weeks
price: contact lab
SPGF9
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany