Number of Panel Genes: 
7

Polycystic liver disease (PCLD) is a rare, autosomal dominant disorder characterized by the presence of isolated liver cysts. To date, mutations in three genes, PRKCSH, SEC63, and LRP5, have been shown to cause PCLD. Even though PCLD is independent of polycystic kidney disease (PKD), hepatic cysts are a common finding in PKD. To aid the differential diagnosis between PCLD and mild PKD cases, PKD genes are included in the panel.

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Tests Available

7 Panel Genes: GANAB, LRP5, PKD1, PKD2, PKHD1, PRKCSH, SEC63
Next Generation Sequencing
$1,220
Test Code: 5339
Deletion / Duplication
$990
Test Code: 5340
NGS/Del Dup Comprehensive
$1,595
Test Code: 5341

Test Details

Technical Information
Panel Genes: 
GANAB, LRP5, PKD1, PKD2, PKHD1, PRKCSH, SEC63
Disease Groups: 
Liver Disorders
Billing
Price: 
$1,220
CPT Codes: 
81406 x 2
81407 x 1
81408 x 1
81479 x 3
Ordering
SKU:
5339
Turnaround Time: 
Typically 2 to 4 weeks from receipt of a sample in the laboratory. All cases involving ongoing pregnancies will be expedited.
Non-Prenatal Specimens: 
  1. Whole blood: purple-top (EDTA) tube, minimum of 3 ml
  2. Genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl)
  3. Fibroblasts: 4 confluent T-25 flasks
  4. Saliva: only samples collected in Oragene DNA Self-Collection Kit or Oragene Saliva Collection Kit for Young Children are accepted
Prenatal Specimens: 
  1. Cultured cells: 4 confluent T-25 flasks derived from amnio or CVS samples
  2. Genomic DNA: a minimum of 3 µg (at a concentration of at least 30 ng/µl)
Shipping: 
Ship all specimen types at room temperature by overnight courier. Do not freeze.

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