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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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GSD Comprehensive Panel by Massively Parallel Sequencing (BCM-MitomeNGSSM)
Test Information: Glycogen storage diseases (GSDs) are a group of inherited genetic defects of glycogen synthesis or catabolism. GSDs are categorized into 15 subtypes, based on the specific enzyme deficiency and disease phenotype. Common symptoms include hypoglycemia, hepatomegaly, developmental delay and muscle cramps. Based on major clinical presentation, GSDs can be divided into two sub-forms: muscle and liver. This comprehensive panel includes genes involved in both the muscle and liver forms of GSDs.
Test Details
Test Code: 2125
Special Notes: Twenty-three nuclear encoded genes involved in the glycogen synthesis or catabolism are analyzed by the newly developed and clinically validated approach of Massively Parallel Sequencing (MPS) using Next Generation Sequence (NGS) technology. The genes analyzed by this panel are tabulated below . Sequencing of these genes is also available using the associated individual test codes.
AGL (#3670), FBP1 (#3935), G6PC (#3130), GAA (#3400), GBE1 (#3825), GYG1 (#29035), GYS1 (#3835), GYS2 (#3530), LAMP2 (#29040), LDHA (#3785), PCK1 (#29045), PCK2 (#29050), PFKM (#3820), PGAM2 (#3805), PGM1 (#2520), PHKA1 (#3985), PHKA2 (#3990) PHKB (#3975), PHKG2 (#3980), PYGL (#3790), PYGM (#3800), SLC2A2 (#29055), and SLC37A4 (#3830).
All coding exons of these 23 nuclear genes and at least 20 base pairs of flanking intronic sequences are analyzed. All exonic variants and intronic variants within 20 bp of the exon/intron boundary will be reported. Sequence analysis will not detect genomic structural rearrangements (e.g. heterozygous deletions, duplications, and inversions), large heterozygous insertion mutations (e.g. ALU mediated insertion), and mutations within the promoter or deep intronic regions. Mutations and novel variants detected by NGS are confirmed by Sanger sequencing.

Mitomet deletion/duplication analysis (#3500) for the genes covered by this panel is also available.
Technical Information
Methodology: Targeted Capture followed by Massively Parallel Sequencing
Gene Name: See "Special Notes" section for list of genes.
Sample & Shipping Information
Test Requisition: Mitochondrial
Specimen Type: Blood
Requirements: Draw blood in an EDTA (purple-top) tube(s) and send 3-5 cc (Adults/Children).
Shipping Conditions: Ship at room temperature in an insulated container by overnight courier. Do not heat or freeze. Sample must arrive within 48 hrs.

Specimen Type: Purified DNA
Requirements: Send at least 5ug of purified DNA (minimal concentration of 50ng/uL; A260/A280 of ~1.7).
Shipping Conditions: Ship at room temperature in an insulated container by overnight courier. Do not heat or freeze.

Turn Around Time: 56 days
Billing Information
List Price: *For Insurance or Institutional Prices, please call.
CPT Codes: 81406x2, 81479x14

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