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TRPM1 Gene Sequencing

FORMS AND DOCUMENTS

TEST DETAILS

Genes:
TRPM1
Disorders:
Clinical Utility:
  • Confirmation of a clinical diagnosis.
  • Development of an appropriate management plan.
  • Prenatal diagnosis in families with a defined mutation
Lab Method:
Capillary Sequencing

ORDERING

Test Code:
489
Turnaround Time:
8-9 weeks
Preferred Specimen:
2-5 mL Blood - Lavender Top Tube

BILLING

CPT Codes:
81479x1
New York Approved:
No
ABN Required:
Yes
Billing Information:
View Billing Policy
ICD Codes:
  • 368.63: Abnormal dark adaptation curve, Abnormal threshold of cones or rods, Delayed adaptation of cones or rods
  • 368.61: Congenital night blindness, Hereditary night blindness, Oguchi's disease
* For price inquiries please email zebras@genedx.com

REFERENCES

  1. van Genderen et al., (2009) Am J Hum Genet 85: 730-736
  2. Audo et al., (2009) Am J Hum Genet 85: 720- 729
  3. Li et al., (2009) Am J Hum Genet 85:711-719
  4. Xiao et al., (2006) J Hum Genet 51:634-640
  5. Pusch et al., (2000) Nat Genet 26:324-327
  6. Bech-Hansen et al., (2000) Nat Genet 26: 319-323

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