SCARF2

OMIMHGNC

Synonym(s): SREC-II, SREC2, HUMZD58C02

Locus: 22q11.21

 

Disorders

Tests

Test Type
Molecular (7)
Multi-Gene Panel (3)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (2)
Sequencing, Capillary (Sanger) (3)
Sequencing, Next Gen (5)
Prenatal/Carrier
Prenatal (1)
Carrier (3)
Lab Location
Portugal(2)
USA(2)
Spain(2)
Germany(1)
 
Distal Arthrogryposis, Massive Sequencing (NGS) 9 Genes
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
Craniosynostosis (NGS panel for 30 genes)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal
Van den Ende-Gupta syndrome (sequence analysis of SCARF2 gene)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal
TAT: 8-9 weeks
price: contact lab
Abnormal/Ambiguous Genitalia Sequencing Test
method(s): ◦ Sequencing, Next Gen 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 4-5 Weeks
price: contact lab
SCARF2
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Van den Ende-Gupta Syndrome, Sequencing SCARF2 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: ~2 weeks
price: contact lab
Van den Ende-Gupta syndrome
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany