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Hyperparathyrodism  – HPT8

This panel is developed for use in cases where hyperparthyrodism is suspected. The genes in the panel are reletad to the following phenotypes, Pituitaryadenoma, prolactin secreting – Multiple endocrineneoplasia, type I + IV – Thyroid carcinoma, papillary – Parathyroid carcinoma – Hypoparathyroidism, familial isolated – Hypocalcemia, autosomal dominant 2 – Hypocalciuric hypercalcemia, familial, type III


The current version includes 8 genes.

Genes list

Name OMIM Inheritance

Test specifications

The test is performed as data extract (virtual targeted panel) from whole exome data.

Chemistry: Twist Biosystems Human Core Exome

Hardware: Illumina Novaseq 6000 Sequencer

Data processing: Variant calling and filtering is performed with an in-house bioinformatic pipeline.

Metrics: Average read depth >100-fold. On target coverage >97% at a >20-fold read depth.



By ordering an analysis at Amplexa Genetics A/S, the requester confirms to have obtained the necessary informed consent for the performance of the requested analyses, and accepts Amplexa Genetics Terms and Conditions. A hard-copy requisition or an e-mail stating the specific analysis together with the receipt of a sample is considered an order to conduct the analysis.

From the day of order receipt the turn around time is 5 weeks.


This test is not part of the accredited workflow.