Connective Tissue Panel
Connective Tissue Panel
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Connective tissue disease here refers to that group of disorders involving the protein-rich tissue that supports organs and other parts of the body, and affecting the parts of the body that connect bodily structures to each other.
The analysis takes into consideration the mutation of germline DNA, it investigates SNP and Indel mutations up to 150 bp.
- Available in less than 24 hours
- Based on Whole Genome Sequencing
- More than 50 genes analyzed
- Investigates SNP and Indel mutations up to 150 bp
List of main conditions:
- Ehlers-Danlos syndrome
- Loeys-Dietz Syndrome 6
- Macs Syndrome
List of genes analyzed:
ABCC6, ACTA2, ADAMTS10, ADAMTS2, ADAMTSL2, ALDH18A1, ATP6V0A2, ATP7A, B3GALT6, B3GAT3, B4GALT7, C1R, C1S, CBS, CHST14, CHST3, COL11A1, COL11A2, COL12A1, COL1A1, COL1A2, COL2A1, COL3A1, COL5A1, COL5A2, COL9A1, COL9A2, COL9A3, DSE, EFEMP2, ELN, FBLN5, FBN1, FBN2, FKBP14, FLNA, FLNB, LTBP4, MED12, MYH11, MYLK, NOTCH1, PKD2, PLOD1, PRDM5, PRKG1, PYCR1, RIN2, SKI, SLC2A10, SLC39A13, SMAD2, SMAD3, SMAD4, TGFB2, TGFB3, TGFBR1, TGFBR2, TNXB, ZNF469

Dieses Produkt ist nur für Kunden gedacht, die bereits einen MyGenome-Test erworben haben.