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HEREDITARY HEARING LOSS AND DEAFNESS (FULL PANEL) , PANEL MASSIVE SEQUENCING (NGS) 107 GENES
| Test Code |
70115 |
|---|---|
| Gene/s |
See all genes  Hide all genes  107 gens |
| Specific Gene |
ABHD12, ACTG1, AIFM1, ALMS1, ATP6V1B1, BSND, CABP2, CCDC50, CDH23, CEACAM16, CHD7, CIB2, CLDN14, CLPP, CLRN1, COCH, COL11A2, COL4A5, COL4A6, CRYM, DIAPH1, DNMT1, DSPP, EDNRB, EPS8, ESPN, ESRRB, EYA1, EYA4, FGF3, GATA3, GIPC3, GJB2, GJB3, GJB6, GPSM2, GRHL2, GRXCR1, GSDME, HGF, HOMER2, HSD17B4, ILDR1, KARS, KCNE1, KCNQ1, KCNQ4, KITLG, LARS2, LHFPL5, LOXHD1, LRTOMT, MARVELD2, MIR96, MITF, MSRB3, MYH14, MYH9, MYO15A, MYO3A, MYO6, MYO7A, OSBPL2, OTOA, OTOF, OTOG, OTOGL, P2RX2, PAX2, PAX3, PCDH15, PDZD7, PJVK, PNPT1, POU3F4, POU4F3, PRPS1, PTPRQ, RDX, SALL1, SALL4, SERAC1, SERPINB6, SIX1, SLC17A8, SLC26A4, SLC26A5, SMPX, SNAI2, SOX10, SOX2, STRC, SYNE4, TBC1D24, TECTA, TIMM8A, TJP2, TMC1, TMIE, TMPRSS3, TNC, TPRN, TRIOBP, USH1C, USH2A, WFS1, WHRN |
| Analysis Methods |
Massive sequencing data analysis (NGS) |
| Sample Requirements |
10 mL whole blood (EDTA). Necessary clinical and family history. |
| TAT |
30 days |
| Omim G |
– |
| Omim F |
– |
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