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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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Carnitine Deficiency, Systemic tests available.

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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) Sequence Analysis
(Prenatal Diagnosis)
Test Information: Prenatal Diagnosis - Known Familial Mutation(s)
Test Details
Test Code: 3362
Test Includes: Sequencing of the region(s) containing the familial alteration(s)

Special Notes: 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.
Technical Information
Methodology: Sequencing analysis of the region(s) containing the familial alteration(s) is performed in the forward and reverse directions
Gene Name: SLC22A5 (OCTN2)
Protein Name: Solute carrier family 22 member 5
Test Type: Sequence Analysis
Sample & Shipping Information
Test Requisition: Prenatal Comprehensive
Specimen Type: Specimen Information
Requirements: Requirements Information
Shipping Conditions: Ship at ambient temperature in an insulated container by overnight courier.

Billing Information
List Price: *For Insurance or Institutional Prices, please call.
CPT Codes: 81403x1, 81265x1, 81266x1


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