RANBP2

OMIMHGNC

Synonym(s): NUP358, ADANE, ANE1

Locus: 2q13

Protein: Putative peptidyl-prolyl cis-trans isomerase

 

Disorders

Tests

Test Type
Molecular (7)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (2)
Sequencing, Capillary (Sanger) (5)
Sequencing, Next Gen (3)
Prenatal/Carrier
Prenatal (3)
Carrier (2)
Lab Location
Spain(1)
USA(2)
Portugal(1)
Germany(3)
 
Familial Acute Necrotizing Encephalopathy , Sequencing RANBP2 Gene
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 4-6 weeks
price: contact lab
RANBP2 Common Mutations Analysis
method(s): ◦ Sequencing, Capillary (Sanger) 
Cincinnati Children's Hospital Medical Center, Molecular Genetics Laboratory - Cincinnati, OH, USA
Encephalopathy, acute necrotizing (sequence analysis of RANBP2 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 3-5 weeks
price: contact lab
RANBP2
method(s): ◦ Sequencing, Capillary (Sanger) 
MGZ München, Medizinisch Genetisches Zentrum München - München, Germany
TAT: 4-5 Weeks
price: contact lab
RANBP2
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
TAT: ~2 weeks
price: contact lab
Encephalopathy acute necrotizing type 1
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany
TAT: 2-3 weeks
price: contact lab
CentoICU Platinum
method(s): ◦ Sequencing, Next Gen 
Centogene AG, Rare Disease Company - Rostock, Germany