3-Methylcrotonyl-CoA Carboxylase Deficiency

 

OMIMRelated Disorders

Test Type
Biochemical (11)
Molecular (7)
Multi-Gene Panel (5)
Multi-Method Panel (5)
Test Method
Qualitative Biochemical Analysis (10)
Del/Dup (CNV) (2)
Mutation Scanning of Select Exons (1)
Mutation Scanning of Entire Coding Region (1)
Quantitative Biochemical Analysis (3)
Sequencing, Capillary (Sanger) (1)
Uniparental Disomy (1)
Sequencing, Next Gen (7)
Chromosome Analysis (1)
Prenatal/Carrier
Prenatal (2)
Carrier (3)
Lab Location
USA(16)
Spain(1)
Canada(1)


Test
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis ◦ Quantitative Biochemical Analysis 
ARUP Laboratories, Biochemical Genetics Laboratory - Salt Lake City, UT, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis 
Denver Genetic Laboratories - Biochemical Genetics at Children's Hospital Colorado - Aurora, CO, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis ◦ Quantitative Biochemical Analysis 
Ichan School of Medicine at Mount Sinai, Mount Sinai Genetic Testing Laboratory-Biochemical Genetics Division - New York, NY, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis 
New York State Institute for Basic Research in Developmental Disabilities, Biochemical Genetics - Staten Island, NY, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis 
University of Alabama Birmingham, Biochemical Genetics Laboratory - Birmingham, AL, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis 
Children's Hospital of Philadelphia, Michael J. Palmieri Metabolic Disease Laboratory - Philadelphia, PA, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis 
University of Maryland, Pediatric Biochemical Genetics Laboratory - Baltimore, MD, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis 
University of Michigan, Michigan Medical Genetics Laboratories - Ann Arbor, MI, USA
TAT: 1 week
price: contact lab
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Quantitative Biochemical Analysis 
Baylor Research Institute, Institute of Metabolic Disease - Dallas, TX, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis 
Emory University School of Medicine, Emory Biochemical Genetics Laboratory - Atlanta, GA, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency Test
method(s): ◦ Qualitative Biochemical Analysis 
Mayo Clinic - Minnesota, Biochemical Genetics Laboratory - Rochester, MN, USA
TAT: 2-3 days
price: contact lab
Baby Genes Newborn Screening Panel
method(s): ◦ Chromosome Analysis ◦ Del/Dup (CNV) ◦ Mutation Scanning of Entire Coding Region ◦ Mutation Scanning of Select Exons ◦ Sequencing, Next Gen ◦ Uniparental Disomy 
Baby Genes Inc - Golden, CO, USA
3-Methylcrotonyl-CoA Carboxylase Deficiency: MCCC1 and MCCC2 genes sequence analysis
method(s): ◦ Sequencing, Next Gen 
GENETAQ, Molecular Genetics Centre - Malaga, Spain
3-Methylcrotonyl-CoA Carboxylase (3-MCC) Deficiency: MCCC1/MCCC2 Gene Sequencing
method(s): ◦ Sequencing, Capillary (Sanger) ◦ Sequencing, Next Gen 
CEN4GEN Institute for Genomics and Molecular Diagnostics - Edmonton, Canada
TAT: 4-6 weeks
price: contact lab
3-Methylcrotonyl-CoA Carboxylase Deficiency NGS Panel
method(s): ◦ Sequencing, Next Gen 
DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA
TAT: 4-6 weeks
price: contact lab
MCCC1 Gene Sequencing
method(s): ◦ Sequencing, Next Gen 
DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA
TAT: 4-6 weeks
price: contact lab
MCCC2 Gene Sequencing
method(s): ◦ Sequencing, Next Gen 
DDC Clinic Molecular Diagnostics Laboratory - Middlefield, OH, USA
TAT: 1-3 weeks
price: $1,500.00
Invitae 3-Methylcrotonyl-CoA Carboxylase Panel
method(s): ◦ Sequencing, Next Gen ◦ Del/Dup (CNV) 
Invitae - San Francisco, CA, USA