Number of Panel Genes: 
16

Heritable dental developmental anomalies include amelogenesis imperfecta (AI), dentinogenesis imperfecta (DI), and dentin dysplasia (DD).  AI, also called congenital enamel hypoplasia, is an inherited defect of dental enamel formation. The teeth are small, discolored, pitted or grooved, and prone to rapid wear and breakage. It affects all or nearly all of the teeth in both the primary and permanent dentitions. DI is a hereditary disorder of dentin formation.read more

Tests Available

16 Panel Genes: AMELX, C4ORF26, DLX3, DSPP, ENAM, FAM20A, FAM83H, GPR68, ITGB6, KLK4, LAMA3, LAMB3, MMP20, SLC24A4, SMOC2, WDR72
Next Generation Sequencing
$1,395
Test Code: 5197
Deletion / Duplication
$990
Test Code: 5198
NGS/Del Dup Comprehensive
$1,770
Test Code: 5199

Test Details

Technical Information
Panel Genes: 
AMELX, C4ORF26, DLX3, DSPP, ENAM, FAM20A, FAM83H, GPR68, ITGB6, KLK4, LAMA3, LAMB3, MMP20, SLC24A4, SMOC2, WDR72
Disease Groups: 
Skin, Tooth, Nail and Hair Disorders
Billing
Price: 
$1,395
CPT Codes: 
81479 x 16
Ordering
SKU:
5197
Turnaround Time: 
Typically 3 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: minimum of 10 µg (at a concentration of at least 50 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: minimum of 10 µg (at a concentration of at least 50 ng/µl)
Shipping: 
Ship all specimen types at room temperature by overnight courier. Do not freeze.

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