NDN

OMIMHGNC

Synonym(s): HsT16328, PWCR

Locus: 15q11.2

Protein: Necdin

Tests

Test Type
Molecular (7)
Multi-Gene Panel (4)
Multi-Method Panel (3)
Test Method
Del/Dup (CNV) (2)
Methylation Analysis (2)
Sequencing, Capillary (Sanger) (3)
Sequencing, Next Gen (3)
Prenatal/Carrier
Prenatal (2)
Carrier (3)
Lab Location
Portugal(1)
USA(2)
Singapore(1)
United Kingdom(1)
Austria(1)
Germany(1)
 
TAT: 1 week
price: contact lab
Prader Willi/Angelman syndrome MS-PCR
method(s): ◦ Methylation Analysis 
Molecular Diagnosis Centre, Department of Laboratory Medicine, National University Hospital - Singapore, Singapore
Prader Willi syndrome
method(s): ◦ Methylation Analysis 
South West Thames Genetics Laboratory, St George's University of London - London, United Kingdom
TAT: 7-10 days
price: contact lab
NewbornDx
method(s): ◦ Sequencing, Next Gen 
Parabase Genomics - Boston, MA, USA
Prader-Willi syndrome (sequence analysis of NDN gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 4-5 Weeks
price: contact lab
NDN
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Prader-Willi syndrome (Prader-Willi Syndrom)
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
Praxis fuer Humangenetik Wien - Vienna, Austria
TAT: ~2 weeks
price: contact lab
Prader-Willi syndrome
method(s): ◦ Sequencing, Capillary (Sanger) 
Centogene AG, Rare Disease Company - Rostock, Germany