SLC52A1

OMIMHGNC

Synonym(s): FLJ10060, GPCR42, PAR2, hRFT1, RFVT1, GPR172B

Locus: 17p13.2

Protein: Solute carrier family 52, riboflavin transporter, member 1

 

Disorders

Tests

Test Type
Molecular (4)
Multi-Gene Panel (2)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (1)
Sequencing, Capillary (Sanger) (2)
Sequencing, Next Gen (3)
Prenatal/Carrier
Prenatal (1)
Carrier (3)
Lab Location
USA(2)
Spain(1)
Germany(1)
 
TAT: 7-10 days
price: contact lab
NewbornDx
method(s): ◦ Sequencing, Next Gen 
Parabase Genomics - Boston, MA, USA
TAT: 4-5 Weeks
price: contact lab
SLC52A1
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Motor Neuron Disorder and Related Diseases, Panel Massive Sequencing (NGS) 49 Genes
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 3-4 weeks
price: contact lab
Riboflavin deficiency
method(s): ◦ Sequencing, Capillary (Sanger) 
Centogene AG, Rare Disease Company - Rostock, Germany