KRT81

OMIMHGNC

Synonym(s): Hb-1, KRTHB1

Locus: 12q13.13

 

Disorders

Tests

Test Type
Molecular (4)
Multi-Gene Panel (3)
Multi-Method Panel (2)
Test Method
Del/Dup (CNV) (1)
Mutation Scanning of Entire Coding Region (1)
Sequencing, Capillary (Sanger) (2)
Sequencing, Next Gen (2)
Prenatal/Carrier
Prenatal (1)
Carrier (2)
Lab Location
Spain(1)
Germany(2)
Poland(1)
 
TAT: 6-7 weeks
price: contact lab
Sanger sequencing of KRT81 and KRT86 genes
method(s): ◦ Mutation Scanning of Entire Coding Region ◦ Sequencing, Capillary (Sanger) 
Sistemas Genomicos, Medical Genetics Unit - Paterna, 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
KRT81
method(s): ◦ Del/Dup (CNV) ◦ Sequencing, Capillary (Sanger) 
University Clinic Freiburg, Institute for Human Genetics - Freiburg, Germany
Ectodermal dysplasia (including hypotrichosis and hypoplastic hair)
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany