• Turnaround time:
    10–21 calendar days (14 days on average)
  • Preferred specimen:
    3mL whole blood in a purple-top tube
  • Alternate specimens:
    DNA or saliva/assisted saliva
  • Sample requirements
  • Request a sample kit



ALC1; AMLC; GT1; MLC1; PRO1957

Associated disorders

The MYL4 gene is associated with autosomal recessive and autosomal dominant atrial fibrillation (PMID: 2580728, 27066836).

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Invitae tests that include this gene:

Pathogenic variants in the MYL4 gene are a rare cause of atrial fibrillation.

The MYL4 gene encodes the embryonic/atrial myosin alkali light chain 4 protein. This protein belongs to the family of myosins and is expressed in both fetal and adult cardiac muscle, where it is a structural component of the muscle sarcomere.

Assay and technical information

Invitae is a College of American Pathologists (CAP)-accredited and Clinical Laboratory Improvement Amendments (CLIA)-certified clinical diagnostic laboratory performing full-gene sequencing and deletion/duplication analysis using next-generation sequencing technology (NGS).

Our sequence analysis covers clinically important regions of each gene, including coding exons, +/- 10 base pairs of adjacent intronic sequence in the transcript listed below. In addition, analysis covers the select non-coding variants specifically defined in the table below. Any variants that fall outside these regions are not analyzed. Any specific limitations in the analysis of these genes are also listed in the table below.

Our analysis detects most intragenic deletions and duplications at single exon resolution. However, in rare situations, single-exon copy number events may not be analyzed due to inherent sequence properties or isolated reduction in data quality. If you are requesting the detection of a specific single-exon copy number variation, please contact Client Services before placing your order.

Gene Transcript reference Sequencing analysis Deletion/Duplication analysis
MYL4 NM_001002841.1