MIR17HG

OMIMHGNC

Synonym(s): FLJ14178, MIRH1, MIHG1, NCRNA00048, miR-17-92, LINC00048, C13orf25, MIRHG1

Locus: 13q31.3

 

Disorders

Tests

Test Type
Molecular (6)
Multi-Gene Panel (1)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (3)
Sequencing, Capillary (Sanger) (4)
Sequencing, Next Gen (2)
Prenatal/Carrier
Carrier (4)
Lab Location
Portugal(1)
USA(2)
Spain(2)
Germany(1)
 
TAT: 2-3 weeks
price: contact lab
Feingold Syndrome 2 Test
method(s): ◦ Del/Dup (CNV) 
Alfred I. duPont Hospital for Children, Molecular Diagnostics Lab - Wilmington, DE, USA
Feingold syndrome 2 (sequence analysis of MIR17HG gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 4-5 Weeks
price: contact lab
MIR17HG
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Facial Dysostosis Related Disorders, Panel Massive Sequencing (NGS) 10 Genes
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 3-4 weeks
price: contact lab
Feingold syndrome type 2
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany
Feingold Syndrome Type 2, Sequencing MIR17HG Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain