KCTD1

OMIMHGNC

Synonym(s): C18orf5

Locus: 18q11.2

Protein: BTB/POZ domain-containing protein KCTD1

 

Disorders

Tests

Test Type
Molecular (3)
Multi-Gene Panel (1)
Multi-Method Panel (1)
Test Method
Del/Dup (CNV) (1)
Sequencing, Capillary (Sanger) (2)
Sequencing, Next Gen (2)
Lab Location
Portugal(1)
USA(1)
Germany(1)
 
Ectodermal dysplasia (including hypotrichosis and hypoplastic hair)
method(s): ◦ Sequencing, Next Gen 
CeGaT GmbH - Tübingen, Germany
TAT: 8-9 weeks
price: contact lab
Scalp-ear-nipple syndrome (sequence analysis of KCTD1 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 4-5 Weeks
price: contact lab
KCTD1
method(s): ◦ Sequencing, Next Gen ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Fulgent Diagnostics - Temple City, CA, USA