SLC1A4

OMIMHGNC

Synonym(s): SATT, ASCT1

Locus: 2p14

 

Disorders

Tests

Test Type
Molecular (7)
Multi-Gene Panel (5)
Multi-Method Panel (3)
Test Method
Del/Dup (CNV) (2)
Sequencing, Capillary (Sanger) (2)
Sequencing, Next Gen (6)
Prenatal/Carrier
Prenatal (2)
Carrier (3)
Lab Location
USA(4)
Germany(3)
 
TAT: 8-9 weeks
price: contact lab
Early Infantile Epileptic Encephalopathy Panel
method(s): ◦ Sequencing, Next Gen 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
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: 4-6 weeks
price: contact lab
Hereditary Spastic Paraplegias (HSP) and Differential Diagnoses Panel
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
TAT: 8-10 weeks
price: contact lab
Epilepsy Exome Panel
method(s): ◦ Sequencing, Next Gen 
University of Chicago, Genetic Services Laboratory - Chicago, IL, USA
TAT: 4-5 Weeks
price: contact lab
SLC1A4
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
TAT: 4-6 weeks
price: contact lab
Hereditary spastic paraplegia (HSP), autosomal recessive and X-linked Panel
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
TAT: 3-4 weeks
price: contact lab
Developmental delay and microcephaly, SLC1A4 related
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany