KRT17

OMIMHGNC

Synonym(s): PCHC1

Locus: 17q21.2

Protein: Keratin, type I cytoskeletal 17

 

Disorders

Tests

Test Type
Molecular (12)
Multi-Gene Panel (5)
Multi-Method Panel (5)
Test Method
Del/Dup (CNV) (3)
Mutation Scanning of Entire Coding Region (1)
Sequencing, Capillary (Sanger) (8)
Sequencing, Next Gen (5)
Prenatal/Carrier
Prenatal (3)
Carrier (5)
Lab Location
Spain(3)
USA(3)
Germany(3)
Portugal(1)
Poland(1)
Finland(1)
 
TAT: 6-7 weeks
price: contact lab
Sanger sequencing of KRT17 gene
method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Capillary (Sanger) 
Sistemas Genomicos, Medical Genetics Unit - Paterna, Spain
TAT: 4-6 weeks
price: contact lab
KRT17 Hot Spots
method(s): ◦ Sequencing, Capillary (Sanger) 
GeneDx - Gaithersburg, MD, USA
TAT: 4-6 weeks
price: contact lab
KRT6B, KRT17 Hot Spots
method(s): ◦ Sequencing, Capillary (Sanger) 
GeneDx - Gaithersburg, MD, USA
Pachyonychia Congenita Type 2, Sequencing KRT17 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
Skin Diseases Panel
method(s): ◦ Sequencing, Next Gen 
Genomic Laboratory of the DNA Research Center LTD (Centrum Badań DNA sp z o.o.) - Poznań, Poland
TAT: 4-6 weeks
price: contact lab
Ichthyoses and Related Disorders of Cornification Panel
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
Steatocystoma multiplex (sequence analysis of KRT17 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 4-5 Weeks
price: contact lab
KRT17
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA
Pachyonychia Congenita, Panel Massive Sequencing (NGS) KRT6A, KRT6B, KRT16, KRT17 Genes
method(s): ◦ Sequencing, Next Gen 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
TAT: 3-4 weeks
price: contact lab
Pachyonychia Congenita Panel
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Next Gen 
Blueprint Genetics - Helsinki, Finland
TAT: 3-4 weeks
price: contact lab
Steatocystoma multiplex
method(s): ◦ Sequencing, Capillary (Sanger) 
Centogene AG, Rare Disease Company - Rostock, Germany
TAT: 3-4 weeks
price: contact lab
Pachyonychia congenita type 2
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany