skip to content »

Pediatrics - Cardiology

Houston, Texas

BCM faculty, staff and trainees are the heart of the organization.
Pediatrics - Cardiology
not shown on screen

KCNJ5 Mutation Analysis

KCNJ5 (potassium inwardly-rectifying channel, subfamily J, member 5) gene contains two exons spanning 26 kb of genomic distance that was mapped to chromosome 11q24. The protein encoded by this gene is an integral membrane protein controlled by G-proteins and inward-rectifier type potassium channel and has a greater tendency to allow potassium to flow into a cell rather than out of a cell. It may associate with two other G-protein-activated potassium channels to form a heteromultimeric pore-forming complex. Defects in KCNJ5 are the cause of long QT syndrome type 13 (LQT13) characterized by a prolonged QT interval on the ECG and polymorphic ventricular arrhythmias. Mutaions in KCNJ5 also lead to familial hyperaldosteronism type III. KCNJ5 mutations demonstrate autosomal dominant inheritance with a broad range of clinical severity both within and between families. Definitive genotype/phenotype correlations have not been described.

The John Welsh Cardiovascular Diagnostic Laboratory offers molecular genetic testing for KCNJ5 mutations. Individuals are tested by automatic fluorescent DNA sequencing of the coding exons of the KCNJ5 gene. We strongly recommend initial testing of a clearly affected individual, if available, in order to provide the greatest test sensitivity and clearest interpretation of results for subsequent family members. Genetic counseling is recommended for all individuals.

Reasons for Referral

Molecular confirmation of the diagnosis of long-QT syndrome type 13 (LQT13) and familial hyperaldosteronism type III.

Methodology

Genomic DNA is analyzed for KCNJ5 mutations by automatic fluorescent DNA sequencing of the coding exons of the KCNJ5 gene, as well as the exon/intron junctions and a portion of the 5' and 3' untranslated region. Patient DNA is sequenced in both the forward and reverse orientations. If a mutation is identified, additional family members are analyzed only for the familial mutation by automatic fluorescent DNA sequencing.

Service Fees

Service Direct and Institutional Billing CPT Codes
Index Case (Male or Female) $600 per sample 81404, G0452
Additional Family Members $300 per sample; known familial mutation only 81403, G0452

Sensitivity

DNA Sequencing Analysis: Approximately 99 percent detection of mutations in the coding exons 2-3 of KCNJ5

Specimen Requirements

Blood (preferred): EDTA (purple-top) tubes: Adult: 5 cc, Child: 5 cc, Infant: 2-3 cc
Tissue: Frozen (preferred), RNAlater, Formalin-fixed, Paraffin-embedded
Other Body Fluids: Call to inquire
Buccal Swabs: One swab from each cheek

Download Printable Version

E-mail this page to a friend