KCNJ18

OMIMHGNC

Synonym(s): KIR2.6, TTPP2

Locus: 17p11.2

Protein: Inward rectifier potassium channel 18

 

Disorders

Tests

Test Type
Molecular (8)
Multi-Gene Panel (4)
Multi-Method Panel (1)
Test Method
Del/Dup (CNV) (1)
Sequencing, Capillary (Sanger) (5)
Sequencing, Next Gen (3)
Prenatal/Carrier
Prenatal (2)
Carrier (4)
Lab Location
USA(2)
Spain(1)
Portugal(2)
Poland(2)
Germany(1)
 
Neuromuscular Diseases Panel
method(s): ◦ Sequencing, Next Gen 
Genomic Laboratory of the DNA Research Center LTD (Centrum Badań DNA sp z o.o.) - Poznań, Poland
Ion Channel Disorders 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
Periodic Paralysis Mutation Screen
method(s): ◦ Sequencing, Capillary (Sanger) 
Mission Health System, Fullerton Genetics Center - Asheville, NC, USA
Hypokalemic Periodic Paralysis , Sequencing KCNJ18 Gene
method(s): ◦ Sequencing, Capillary (Sanger) 
Reference Laboratory Genetics - Hospitalet de Llobregat, Spain
Non-dystrophic myotonias (NGS panel for 11 genes)
method(s): ◦ Sequencing, Next Gen 
CGC Genetics - Porto, Portugal
Thyrotoxic periodic paralysis type 2 (sequence analysis of KCNJ18 gene)
method(s): ◦ Sequencing, Capillary (Sanger) 
CGC Genetics - Porto, Portugal
TAT: 11-12 weeks
price: contact lab
KCNJ18 Gene Sequencing
method(s): ◦ Sequencing, Capillary (Sanger) 
Cincinnati Children's Hospital Medical Center, Molecular Genetics Laboratory - Cincinnati, OH, USA
TAT: ~2 weeks
price: contact lab
Thyrotoxic periodic paralysis type 2
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Del/Dup (CNV) 
Centogene AG, Rare Disease Company - Rostock, Germany