SEMA3A

OMIMHGNC

Synonym(s): SEMA1, SemD, coll-1, Hsema-I, SEMAD

Locus: 7q21.11

Protein: Putative uncharacterized protein SEMA3A

 

Disorders

Tests

Test Type
Molecular (8)
Multi-Gene Panel (5)
Multi-Method Panel (3)
Test Method
Del/Dup (CNV) (3)
Sequencing, Capillary (Sanger) (4)
Sequencing, Next Gen (6)
Prenatal/Carrier
Prenatal (3)
Carrier (2)
Lab Location
Portugal(1)
Germany(1)
Spain(2)
USA(3)
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 16 with or without anosmia (sequence analysis of SEMA3A gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
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: 4-6 Weeks
price: contact lab
Kallmann Syndrome NGS Panel
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
TAT: 4-5 Weeks
price: contact lab
SEMA3A
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
Kallmann syndrome, SEMA3A related
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany