• 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



FPN1; HFE4; IREG1; MST079; MSTP079; MTP1; SLC11A3

Associated disorders

The SLC40A1 gene is associated with autosomal dominant hemochromatosis type 4 (HFE4) (aka ferroportin disease) (MedGen UID: 340044).

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Invitae tests that include this gene:

The percentage of hemochromatosis attributed to pathogenic variants identified in SLC40A1 is unknown.

The SLC40A1 gene encodes for the solute carrier family 40 member 1 protein, which is involved in iron export from the duodenal epithelial cells.

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
SLC40A1 NM_014585.5