SLC38A8

OMIMHGNC

Locus: 16q23.3

Protein: Putative sodium-coupled neutral amino acid transporter 8

 

Disorders

Tests

Test Type
Molecular (6)
Multi-Gene Panel (4)
Test Method
Sequencing, Capillary (Sanger) (2)
Sequencing, Next Gen (4)
Prenatal/Carrier
Prenatal (1)
Carrier (2)
Lab Location
Spain(1)
USA(1)
Germany(2)
Austria(1)
Estonia(1)
 
TAT: 7-8 weeks
price: contact lab
Anterior Segment Dysgenesis, Axenfeld-Rieger Syndrome
method(s): ◦ Sequencing, Next Gen 
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany
TAT: 3-5 weeks
price: contact lab
Ocular / Oculocutaneous Albinism
method(s): ◦ Sequencing, Next Gen 
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany
Foveal Hypoplasia Type 2, Sequencing SLC38A8 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 2-3 weeks
price: $840.00
Isolated Foveal Hypoplasia Type 2 (FVH2) via the SLC38A8 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
PreventionGenetics (Prevention Genetics), Clinical DNA Testing and DNA Banking - Marshfield, WI, USA
Foveal hyperplasia (Foveale Hypoplasie)
method(s): ◦ Sequencing, Next Gen 
Praxis fuer Humangenetik Wien - Vienna, Austria
Anophthalmia/Microphthalmia/Coloboma/Anterior Segment Dysgenesis
method(s): ◦ Sequencing, Next Gen 
Asper Biotech Ltd., Asper Biotech - Tartu, Estonia