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Genetic Labs

Houston, Texas

Genetic Laboratory
Baylor Genetics Laboratories
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Medical Genetics Test Details

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The American Medical Association (AMA) Current Procedural Terminology (CPT) codes and Healthcare Common Procedure Coding System (HCPCS) codes listed, are provided for informational purposes only. The codes reflect our interpretation of CPT/HCPCS coding requirements based upon AMA guidelines published annually. CPT/HCPCS codes are provided only as guidance to assist clients with billing. Baylor Genetics strongly recommends that clients confirm CPT/HCPCS codes with their Medicare Administrative Contractor (MAC) or other payer being billed, as requirements may differ. CPT coding is the sole responsibility of the billing party. Baylor Genetics assumes no responsibility for billing errors due to reliance on the CPT codes listed. Please direct any questions regarding CPT coding to the payer being billed.
Carnitine Deficiency, Systemic (SLC22A5, OCTN2) tests available.

Carnitine Deficiency Primary | Systemic Carnitine Deficiency

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Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing
Deletion/Duplication Analysis SLC22A5 (OCTN2) Deletion/Duplication Analysis
Test Code: 3363
Sequence & Deletion/Duplication Analysis SLC22A5 (OCTN2) Comprehensive - Sequence & Deletion/Duplication Analysis
Test Code: 3364
Sequence Analysis SLC22A5 (OCTN2) Sequence Analysis
Test Code: 3360
SLC22A5 (OCTN2) Sequence Analysis
Test Code: 3361

This test can only be performed if there is a previously identified familial mutation.
SLC22A5 (OCTN2) Sequence Analysis
Test Code: 3362

We require that the referring center consult with our laboratory genetic counselors regarding prenatal cases prior to submitting any samples. Please call 1-800-411-4363.


SLC22A5 (OCTN2) Comprehensive - Sequence & Deletion/Duplication Analysis
Test Information: Confirmation of Clinical Diagnosis
Test Details
Test Code: 3364
Test Includes: Sequence and Deletion/Duplication Analysis of SLC22A5 gene

Special Notes: If the mutation to be tested in this individual is one previously identified in an affected family member, please order test (#3361) for point mutations or (#3363) for duplication and deletion analysis. Please see detailed requirements under these test codes.
Technical Information
Methodology: Sequence analysis is performed in both forward and reverse directions and deletion/duplication analysis performed using a custom designed gene centric microarray.
Gene Name: SLC22A5 (OCTN2)
Protein Name: Solute carrier family 22 member 5
Test Type: Sequence & Deletion/Duplication Analysis
Sample & Shipping Information
Test Requisition: Molecular Diagnostics
Specimen Type: Blood
Requirements: Draw blood in an EDTA (purple-top) tube(s) and send 3-5 cc (Adults/Children) and 3 cc (Infant<2yrs).
Shipping Conditions: Ship at room temperature in an insulated container by overnight courier. Do not heat or freeze.

Turn Around Time: 28 days
Billing Information
List Price: *For Insurance or Institutional Prices, please call.
CPT Codes: 81405x1, 81479x1


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