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  • Turnaround time:
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  • Preferred specimen:
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  • Alternate specimens:
    DNA or saliva/assisted saliva
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RANGRF

Alias

HSPC165; HSPC236; MOG1; RANGNRF

Associated disorders

The RANGRF gene currently has no well-established disease association; however there is preliminary evidence supporting a correlation with autosomal dominant Brugada syndrome (BrS) (PMID: 24142675).

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RANGRF

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Invitae tests that include this gene:

Pathogenic RANGRF variants are associated with an unknown percentage of clinical cases of BrS.

The RANGRF gene encodes the MOG1 protein, which is a co-factor that regulates the expression and function of the cardiac sodium channel Nav1.5.

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
RANGRF NM_016492.4