WDR11

OMIMHGNC

Synonym(s): KIAA1351, FLJ10506, WDR15, HH14, DR11, SRI1, BRWD2

Locus: 10q26.12

 

Disorders

Tests

Test Type
Molecular (7)
Multi-Gene Panel (4)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (2)
Sequencing, Capillary (Sanger) (2)
Sequencing, Next Gen (6)
Prenatal/Carrier
Prenatal (3)
Carrier (2)
Lab Location
Portugal(1)
Spain(2)
USA(2)
Germany(1)
Austria(1)
 
Kallmann Syndrome, Panel Massive Sequencing (NGS) 20 Genes
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
Kallmann Syndrome
method(s): ◦ Sequencing, Next Gen 
GENETAQ, Molecular Genetics Centre - Malaga, Spain
Hypogonadotropic hypogonadism 14 with or without anosmia (sequence analysis of WDR11 gene)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal
TAT: 8-9 weeks
price: contact lab
Hypogonadotropic Hypogonadism Sequencing Panel
method(s): ◦ Sequencing, Next Gen 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 4-5 Weeks
price: contact lab
WDR11
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Kallmann syndrome/ Hypogonadotropic hypogonadism (Kallmann Syndrom)
method(s): ◦ Sequencing, Next Gen 
Praxis fuer Humangenetik Wien - Vienna, Austria
TAT: ~2 weeks
price: contact lab
Hypogonadtropic hypogonadism type 14
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany