Medical Genetics Test Details
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3 - Methylcrotonyl-CoA Carboxylase Deficiency - MCCC1 Related tests available.
3-Methylcrotonyl-CoA Carboxylase Deficiency
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| Diagnostic Testing | Familial Mutation/Variant Analysis | Mutation Testing General Population | Prenatal Diagnosis | Presymptomatic Testing | |
|---|---|---|---|---|---|
| Deletion/Duplication Analysis |
 MCCC1 Deletion/Duplication AnalysisTest Code: 3638 |
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| Sequence & Deletion/Duplication Analysis |
 MCCC1 Comprehensive - Sequence & Deletion/Duplication AnalysisTest Code: 3639 |
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| Sequence Analysis |
MCCC1 Sequence Analysis Test Code: 3635 |
MCCC1 Sequence Analysis Test Code: 3636 This test can only be performed if there is a previously identified familial mutation. |
MCCC1 Sequence Analysis Test Code: 3637 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. |
| MCCC1 Deletion/Duplication Analysis | ||
|---|---|---|
| Test Information: | Confirmation of Clinical Diagnosis, Carrier testing | |
| Test Details | ||
| Test Code: | 3638 | |
| Technical Information | ||
| Methodology: | Deletion/duplication analysis performed using a custom designed gene centric microarray. | |
| Gene Name: | MCCC1 | |
| Protein Name: | Methylcrotonoyl-CoA carboxylase subunit alpha, mitochondrial | |
| Test Type: | 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). | |
| 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: | 81479x1 | |