Name:
Comprehensive panel muscular dystrophy & congenital myopathy Area:
Neurology
GENES:
129
TARGETED PANELS PORTOFLIO / Neurology
Comprehensive panel muscular dystrophy & congenital myopathy
GENES
- ACTA1
- ACTN2
- ADSSL1
- ANO5
- ATP2A1
- B3GALNT2
- B4GAT1
- BAG3
- BIN1
- CACNA1S
- CAPN3
- CASQ1
- CAV3
- CCDC78
- CFL2
- CHKB
- CNTN1
- COL12A1
- COL4A1
- COL6A1
- COL6A2
- COL6A3
- CRYAB
- DAG1
- DES
- DMD
- DNAJB6
- DNM2
- DOK7
- DOLK
- DPM1
- DPM2
- DPM3
- DYSF
- ECEL1
- EMD
- EPG5
- FDX1L(FDX2)
- FHL1
- FKBP14
- FKRP
- FKTN
- FLNC
- FXR1
- GMPPB
- GOLGA2
- HACD1
- INPP5K
- ISPD
- ITGA7
- KBTBD13
- KLHL40
- KLHL41
- KY
- LAMA2
- LAMP2
- LARGE(LARGE1)
- LARGE1
- LDB3
- LIMS2
- LMNA
- LMOD3
- MAP3K20
- MEGF10
- MICU1
- MSTO1
- MTM1
- MTMR14
- MYBPC1
- MYBPC3
- MYF5
- MYH2
- MYH3
- MYH7
- MYH8
- MYL1
- MYMK
- MYO18B
- MYOT
- MYPN
- NEB
- NEFL
- ORAI1
- PABPN1
- PAX7
- PIEZO2
- PLEC
- PNPLA2
- POGLUT1
- POMGNT1
- POMGNT2
- POMK
- POMT1
- POMT2
- PPA2
- PYROXD1
- RBCK1
- RYR1
- RYR3
- SCN4A
- SELENON
- SGCA
- SGCB
- SGCD
- SGCG
- SIL1
- SLC25A4
- SMCHD1
- SPEG
- SPTBN4
- STAC3
- STIM1
- SYNE1
- TCAP
- TMEM43
- TMEM5
- TNNI2
- TNNT1
- TNNT3
- TNPO3
- TOR1AIP1
- TPM2
- TPM3
- TRAPPC11
- TRDN
- TRIM32
- TRIP4
- TTN
- VMA21
