Number of Panel Genes: 
31

Nephrolithiasis is a common condition affecting about 5 to 10% of individuals worldwide. It is multi factorial caused by both genetic and non-genetic factors including dietary and environmental factors. Mutations in the genes currently linked to nephrolithiasis are estimated to be responsible for about 15% of kidney stone cases.

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Tests Available

31 Panel Genes: ADCY10, AGXT, AP2S1, APRT, ATP6V0A4, ATP6V1B1, CA2, CASR, CLCN5, CLDN16, CLDN19, CYP24A1, FAM20A, GNA11, GRHPR, HNF4A, HOGA1, HPRT1, KCNJ1, OCRL, SLC2A9, SLC3A1, SLC4A1, SLC7A9, SLC9A3R1, SLC12A1, SLC22A12, SLC26A1, SLC34A1, SLC34A3, XDH
Next Generation Sequencing
$1,520
Test Code: 5333
Deletion / Duplication
$990
Test Code: 5334
NGS/Del Dup Comprehensive
$1,895
Test Code: 5335

Test Details

Technical Information
Panel Genes: 
ADCY10, AGXT, AP2S1, APRT, ATP6V0A4, ATP6V1B1, CA2, CASR, CLCN5, CLDN16, CLDN19, CYP24A1, FAM20A, GNA11, GRHPR, HNF4A, HOGA1, HPRT1, KCNJ1, OCRL, SLC2A9, SLC3A1, SLC4A1, SLC7A9, SLC9A3R1, SLC12A1, SLC22A12, SLC26A1, SLC34A1, SLC34A3, XDH
Disease Groups: 
Kidney Disorders
Billing
Price: 
$1,520
CPT Codes: 
81404 x 1
81405 x 1
81406 x 1
81407 x 1
81479 x 27
Ordering
SKU:
5333
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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