X-linked mental retardation, NGS


Diagnose genetic causes of X-linked intellectual disability; precise diagnosis and genetic counseling.
Genelist (161): ABCD1, ACSL4, AFF2, AGTR2, AIFM1, ALG13, AMMECR1, AP1S2, ARHGEF6, ARHGEF9, ARSL, ARX, ATP6AP2, ATP7A, ATRX, BCAP31, BCOR, BCORL1, BRWD3, CASK, CCDC22, CDK16, CDKL5, CLCN4, CLIC2, CNKSR2, CTDP1, CUL4B, DCX, DDX3X, DKC1, DLG3, DMD, EBP, EIF2S3, ELK1, EMD, FAAH2, FAM50A, FANCB, FGD1, FHL1, FLNA, FMR1, FRMPD4, FTSJ1, GAN, GDI1, GK, GPC3, GPKOW, GRIA3, GRIPAP1, GSPT2, HCCS, HCFC1, HDAC6, HDAC8, HMGB3, HNRNPH2, HPRT1, HSD17B10, HUWE1, HYCC1, IDS, IGBP1, IKBKG, IL1RAPL1, IQSEC2, KDM5C, KDM6A, KIF4A, KLF8, KLHL15, L1CAM, LAMP2, LAS1L, MAGT1, MAOA, MBTPS2, MECP2, MED12, MID1, MID2, MSL3, MTM1, NAA10, NDP, NDUFA1, NEXMIF, NEXMIF, NHS, NKAP, NLGN3, NLGN4X, NONO, NSDHL, NXF5, OCRL, OFD1, OGT, OPHN1, OTC, PAK3, PCDH19, PDHA1, PGK1, PHF6, PHF8, PIGA, PLP1, POLA1, PORCN, PQBP1, PRPS1, PTCHD1, RAB39B, RAB40AL, RBM10, RBMX, RLIM, RNF113A, RPL10, RPS6KA3, SHROOM4, SLC12A6, SLC16A2, SLC35A2, SLC6A8, SLC9A6, SLC9A7, SMC1A, SMS, SOX3, SRPX2, SSR4, STAG2, STEEP1, SYN1, SYP, TAF1, THOC2, TIMM8A, TmLHE, TSPAN7, UBE2A, UPF3B, USP27X, USP9X, WDR13, WDR45, ZC4H2, ZCCHC12, ZDHHC15, ZDHHC9, ZFP92, ZMYM3, ZNF41, ZNF674, ZNF711, ZNF81