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Genetic Labs

Houston, Texas

Genetic Laboratory
Medical Genetics Laboratories
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Medical Genetics Test Details

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Leber Congenital Amaurosis, Potassium Inwardly-Rectifying Channel, Subfamily J, Member 13 Deficiency tests available.

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Diagnostic Testing Familial Mutation/Variant Analysis Mutation Testing General Population Prenatal Diagnosis Presymptomatic Testing
Deletion/Duplication Analysis KCNJ13 Deletion/Duplication Analysis
Test Code: 5078
Sequence & Deletion/Duplication Analysis KCNJ13 Comprehensive - Sequence & Deletion/Duplication Analysis
Test Code: 5079
Sequence Analysis KCNJ13 Sequence Analysis
Test Code: 5075
KCNJ13 Sequence Analysis
Test Code: 5076

This test can only be performed if there is a previously identified familial mutation.
KCNJ13 Sequence Analysis
Test Code: 5077

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.


KCNJ13 Deletion/Duplication Analysis
Test Information: Confirmation of Clinical Diagnosis
Test Details
Test Code: 5078
Technical Information
Methodology: Deletion/duplication analysis performed using a custom designed gene centric microarray.
Gene Name: KCNJ13
Protein Name: POTASSIUM CHANNEL, INWARDLY RECTIFYING, SUBFAMILY J, MEMBER 13
Test Type: Deletion/Duplication Analysis
Turn Around Time: 28 days
Billing Information
List Price: *For Insurance or Institutional Prices, please call.
CPT Codes: 81479 x 1


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