|
CAKUT |
Painel por Sequenciamento de Próxima Geração |
ACE, AGT, AGTR1, ANOS1, ATRX, BMP4, CBP, CHD1L, CHD7, DHCR7, DSTYK, EP300, ESCO2, EVC, EVC2, EYA1, FGF20, FRAS1, FREM1, FREM2, GATA3, GLI3, GPC-3, GREB1L, HNF1B, HNF1, HSPG2, ITGA8, JAG1, KAL1, KAL2, KIF14, MKS1, MKS4, MUC1, NIPBL, NRIP1, NS1, PAX2, PBX1, PEX, REN, RET, ROBO2, SALL1, SALL4, SIX1, SIX2, SIX5, SOX17, TBX18, TNXB, TRAP1, UMOD, UPK3A, VANGL1, WNT4, WT1 |
|
Microftalmia e Anoftalmia |
Painel por Sequenciamento de Próxima Geração |
SOX2, SHH, RAX, RARB, PXDN, PRSS56, PAX2, OTX2, MFRP, PITX2, MAB21L2, GDF6, FOXE3, ALDH1A3, BCOR, BMP4, HESX1, SALL4, VAX1, GDF3, STRA6, VSX2 |
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Fibrose Congênita dos Músculos Extraoculares |
Painel por Sequenciamento de Próxima Geração |
KIF21A, TUBB3, ARIX, MAFB, CHN1, TUBB2B, HOXA1, SALL4, COL25A1 |
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Ectrodactilia |
Painel por Sequenciamento de Próxima Geração |
SALL4, TP63, SEM1, DLX5, DLX6, FGF8, FGFR1, WNT10B, BHLHA9 |
|
Displasia Esquelética |
Painel por Sequenciamento de Próxima Geração |
ACAN, ACP5, AGPS, ALPL, ANKH, ANO5, ARHGAP31, ARSE, ATP6V0A2, B3GALT6, B4GALT7, BMP2, BMPR1B, CA2, CANT1, CASR, CC2D2A, CDH3, CDKN1C, CEP290, CHST14, CHST3, CHSY1, CLCN5, CLCN7, COL10A1, COL11A1, COL11A2, COL1A1, COL1A2, COL2A1, COL9A1, COL9A2, COL9A3, COMP, CRTAP, CTSK, CUL7, DDR2, DHCR24, DLL3, DLX3, DMP1, DYM, DYNC2H1, EBP, EIF2AK3, ENPP1, ESCO2, EVC, EVC2, EXT1, EXT2, FAM20C, FBLN1, FBN1, FBXW4, FERMT3, FGF10, FGF23, FGFR1, FGFR2, FGFR3, FKBP10, FLNA, FLNB, FMN1, GALNT3, GDF5, GLI3, GNAS, GORAB, GPC6, GREM1, HDAC4, HES7, HOXD13, HPGD, HSPG2, ICK, IFITM5, IFT122, IFT140, IFT80, IHH, KIF22, KIF7, LEMD3, LFNG, LIFR, LMBR1, LMNA, LRP4, LRP5, MAFB, MATN3, MESP2, MGP, MKS1, MMP13, MMP2, MMP9, MYCN, NEK1, NIPBL, NKX3-2, NOG, NOTCH2, NPR2, OBSL1, OSTM1, P3H1, PAPSS2, PCNT, PHEX, PIGV, PITX1, PLOD2, PPIB, PRKAR1A, PTH1R, PTHLH, PTPN11, PYCR1, RASGRP2, RECQL4, ROR2, RPGRIP1L, RUNX2, SALL1, SALL4, SERPINF1, SERPINH1, SH3PXD2B, SHH, SHOX, SLC26A2, SLC34A3, SLC35D1, SLC39A13, SMARCAL1, SOST, SOX9, SP7, SULF1, TBCE, TB |
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Duane-Radial Ray, Síndrome |
Sequenciamento Completo do Gene |
SALL4 |
