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三、高通量测序基因检测试剂盒
技术参数
1. *生产高通量基因测序试剂盒的实验室必须通过 CLIA Lab 认证,或者高通量基因测
序试盒产品通过美国 FDA 或中国 CFDA 认证,具备 8 年以上高通量基因测序试剂盒
生产研发经验。
2. *高通量基因测序试剂盒对已知突变靶基因的测序覆盖率和正确率达到 99.5%以
上。
3. *高通量基因测序试剂盒得到国家认可的基因测序应用示范中心平台和国内外知名
科研机构及三甲医院的应用和推广,通过领域内技术专家和法律专家的论证。
4. *销售高通量基因测序试剂盒的代理商或试剂公司应具备 5 年以上销售及研发经历
可以对售后提供技术支持,探针的设计和数量增减及数据分析。参与过国家重大科
研项目,获得过国家自然基金的资助,在 SCI 上发表过数十篇以上高通量基因测序
相关文章。
5. *销售高通量基因测序试剂盒的代理商或试剂公司应具备三类医疗器械销售资质,
医疗机构执业许可证,临床基因扩增检验实验室技术验收合格证书。
6.*高通量基因测序试剂盒应具备以下组成
高通量基因测序试剂盒
DNA extraction kit
End repair buffer
DNA End Repair Enzyme Mix
dA tailing buffer
dA tailing enzyme
Ligation buffer
Ligation enzyme
Primer PE1.0
Primer PE2.0
Adaptors
Pre-PCR Master Mix
Index Primer1
Index Primer2
Index Primer3
Index Primer4
Index Primer5
Index Primer6
Index Primer7
Index Primer8
Index Primer9
Index Primer10
Index Primer11
Index Primer12
Index Primer13
Index Primer14
Index Primer15
Index Primer16
Index Primer17
Index Primer18
Index Primer19
Index Primer20
Index Primer21
Index Primer22
Index Primer23
Index Primer24
Index Primer25
Index Primer26
Index Primer27
Index Primer28
Index Primer29
Index Primer30
Index Primer31
Index Primer32
Index Primer33
Index Primer34
Index Primer35
Index Primer36
Index Primer37
Index Primer38
Index Primer39
Index Primer40
Index Primer42
Index Primer43
Index Primer44
Index Primer45
Index Primer46
Index Primer47
Index Primer48
Human TGC Probes
Block mixture1
Block mixture2
Block mixture3
Block mixture4
2 x Bead Wash Buffer
Post Hyb Amplification Primers
qPCR-Human TGC Primers1
qPCR-Human TGC Primers 2
Hybridization Buffer1
Hybridization Buffer2
Hybridization Buffer3
Hybridization Buffer4
Wash Reagent 1
Wash Reagent 2
Wash Reagent 3
Magnetic Beads based nucleic acid purification kits
Streptavidin Magnetic Beads
Post-PCR Master Mix
Elution buffer
Neutralization buffer
癌症基因检测
ABCC6, ABI1, ABL1, ABL2, ACSL3,
ACSL6, AFF1, AFF3, AFF4, AIP,
AKAP9, AKT1, AKT2, AKT3, ALDH2,
ALK, APC, AR, ARHGAP26, ARHGEF12,
ARID1A, ARID1B, ARID2, ARID3A,
ARID3B, ARID4A, ARID4B, ARID5A,
ARID5B, ARNT, ASPSCR1, ASXL1,
ATF1, ATIC, ATM, ATR, ATRX,
AURKA, AXIN2
NACA, NBN, NCKIPSD, NCOA1, NCOA2,
NCOA4, NDRG1, NF1, NF2, NFE2L2,
NFIB, NFKB2, NIN, NKX2-1, NONO,
NOTCH1, NOTCH2, NOTCH3, NOTCH4,
NPM1, NR4A3, NRAS, NSD1, NTRK1,
NTRK2, NTRK3, NUMA1, NUP214,
NUP98
BAP1, BCL10, BCL11A, BCL11B,
BCL2, BCL3, BCL6, BCL7A, BCL9,
BCOR, BCR, BIRC3, BLID, BLM,
BMPR1A, BRAF, BRCA1, BRCA2, BRD3,
BRD4, BRIP1, BTG1, BUB1B
OLIG2, OMD, OPTN
C15orf55, CANT1, CARD11, CARS,
CASC5, CBFA2T3, CBFB, CBL, CBLB,
CBLC, CCDC6, CCNB1IP1, CCND1,
CCND2, CCND3, CCNE1, CD274, CD74,
CD79A, CD79B, CDC73, CDH1, CDH11,
CDH6, CDK12, CDK2AP2, CDK4, CDK6,
CDK8, CDKN1A, CDKN1B, CDKN2A,
CDKN2B, CDKN2C, CDKN2D, CDX2,
CEBPA, CHCHD7, CHD5, CHD6, CHEK1,
CHEK2, CHIC2, CHN1, CIC, CIITA,
CLP1, CLTC, CLTCL1, CNBP, CNTRL,
COL1A1, COX6C, CREB1, CREB3L1,
CREB3L2, CREBBP, CRKL, CRLF2,
CRTC1, CRTC3, CSF1R, CTNNB1,
CXCR7, CYLD, CYP1B1
P2RY8, PAFAH1B2, PAK7, PALB2,
PALLD, PATZ1, PAX2, PAX3, PAX5,
PAX6, PAX7, PAX8, PBRM1, PBX1,
PCM1, PCSK7, PDCD1LG2, PDE4DIP,
PDGFB, PDGFRA, PDGFRB, PDPK1,
PER1, PHF6, PHOX2B, PICALM,
PIK3CA, PIK3R1, PIM1, PLAG1,
PLK1, PML, PMS1, PMS2, POU2AF1,
POU5F1, PPARG, PPP2R1A, PRCC,
PRDM1, PRDM16, PRF1, PRKAR1A,
PRKDC, PRRX1, PSIP1, PTCH1, PTEN,
PTK2, PTK2B, PTPN11, PTPRD
DAXX, DDB2, DDIT3, DDX10, DDX5,
DDX6, DEK, DICER1, DNMT3A, DUX4,
RABEP1, RAD51B, RAF1, RALGDS,
RANBP17, RAP1GDS1, RARA, RB1,
RBM15, RECQL4, REL, RET, RHOH,
RICTOR, RMI2, RNASEL, ROS1,
RPL22, RPN1, RPTOR, RRM1, RUNX1,
RUNX1T1
EBF1, EGFR, EIF4A2, ELAC2, ELF4,
ELK4, ELL, ELN, EML4, EP300,
EPCAM, EPHA10, EPHA3, EPHA5,
EPHA6, EPHB6, EPS15, ERBB2,
ERBB3, ERBB4, ERC1, ERCC1, ERCC2,
SARDH, SBDS, SDHAF2, SDHB, SDHC,
SDHD, septin 5, septin 6, septin
9, SET, SETD2, SETDB1, SF3B1,
SF3B2, SFPQ, SH3GL1, SLC45A3,
SMAD2, SMAD3, SMAD4, SMARCA4,
ERCC3, ERCC4, ERCC5, ERG, ETV1,
ETV4, ETV5, ETV6, EWSR1, EXT1,
EXT2, EZH2
SMARCB1, SMO, SNX29, SOCS1, SOX2,
SPECC1, SPEN, SRC, SRD5A2,
SRGAP3, SRSF2, SRSF3, SS18,
SS18L1, SSX1, SSX2, SSX4, STAT3,
STIL, STK11, STX11, STXBP2, SUFU,
SUZ12, SYK
FAM123B, FAM22A, FAM22B, FAM46C,
FANCA, FANCC, FANCD2, FANCE,
FANCF, FANCG, FAS, FBXO11, FBXW7,
FCGR2B, FCRL4, FEV, FGF23, FGFR1,
FGFR1OP, FGFR2, FGFR3, FGFR4, FH,
FHIT, FHL1, FIP1L1, FKBP1B,
FKBP9, FLCN, FLI1, FLT1, FLT3,
FLT4, FNBP1, FOLR1, FOXC1, FOXL2,
FOXO1, FOXO3, FOXO4, FOXP1,
FSTL3, FUBP1, FUS
TAF15, TAL1, TAL2, TCEA1,
TCEA1P2, TCF12, TCF3, TCF4,
TCF7L2, TCL1A, TCL6, TERT, TET1,
TET2, TFE3, TFEB, TFG, TFPT,
TFRC, TGFBR2, THRAP3, TLX1, TLX3,
TMEM127, TMPRSS2, TNFAIP3,
TNFRSF14, TNFRSF17, TOP1, TOP2A,
TP53, TPM3, TPM4, TPR, TRIM24,
TRIM27, TRIM33, TRIP11, TSC1,
TSC2, TSHR, TTL, TYK2
HECW1, HERPUD1, HEY1, HIP1,
HIST1H4I, HLF, HMGA1, HMGA2,
HMGN2P46, HNF1A, HNRNPA2B1,
HOOK3, HOXA11, HOXA13, HOXA9,
HOXC11, HOXC13, HOXD11, HOXD13,
HRAS, HSD17B3, HSD3B2, HSP90AA1,
HSP90AB1
U2AF1, UNC13D, USP6, UTY
IDH1, IDH2, IGF1R, IKBKE, IKZF1,
IL2, IL21R, IL6ST, IL7R, IRF4,
ITK
VHL, VTI1A,
JAK1, JAK2, JAK3, JAZF1, JUN WAS, WDR36, WHSC1, WHSC1L1, WIF1,
WRN, WT1,
KAT6A, KAT6B, KDM5A, KDM5C,
KDM6A, KDR, KDSR, KEAP1,
KIAA1549, KIF1B, KIT, KL, KLF6,
KLK2, KRAS, KRT17, KTN1
XPA, XPC, XPO1,
LASP1, LCK, LCP1, LHFP, LIFR,
LMO1, LMO2, LPP, LRP5, LTBP2,
LTBP3, LYL1
YWHAE,
MAD2L1BP, MAF, MAFB, MALAT1,
MALT1, MAML2, MAP2K1, MAP2K2,
MAP2K4, MAP3K1, MAP3K8, MAX,
MC1R, MCL1, MDM2, MDM4, MDS2,
ZBTB16, ZMYM2, ZNF331, ZNF384,
ZNF521, ZNF668, ZRSR2
MECOM, MED12, MEN1, MET, MITF,
MKL1, MLF1, MLH1, MLL, MLL2,
MLL3, MLLT1, MLLT10, MLLT11,
MLLT3, MLLT4, MLLT6, MN1, MNX1,
MPL, MRE11A, MSH2, MSH6, MSI2,
MSN, MTCP1, MTCP1NB, MTOR, MTUS2,
MUC1, MUTYH, MYB, MYC, MYCL1,
MYCN, MYD88, MYH11, MYH9, MYOC
肺癌靶向基因检测
靶向(全外显子) 化疗基因(部分 SNP 位点)
AKT1 CDA
ALK CYP2B6
BRAF CYP2C9
DDR2 CYP2D6
EGFR DPYD
FGFR1 DYNC2H1
ERBB2 ERCC1
KRAS ERCC2
MAP2K1 GSTP1
MET GSTT1
NRAS ABCB1(MDR1)
NTRK1 MnSOD
PIK3CA MTHFR
PTEN RRM1
RET TEKT4
ROS1 TPMT
RICTOR TYMS
FGFR3 UGT1A1
XPC
XRCC1
NQO1
甲状腺癌基因检测
基因 突变或融合
BRAF 599, 600, 601
KRAS 12, 13
NRAS 61
HRAS 62
PAX8/PPARG 基因融合的区域
RET/NCOA4 基因融合的区域
RET/CCDC6 基因融合的区域
结直肠癌基因检测
基因名 名称及信息描述 NCBI 编码
APC Adenomatous polyposis coli NM_000038.5
BMPR1A Bone morphogenetic protein receptor,
type IA
NM_004329.2
CDH1 Cadherin-1 , CAM 120/80 , epithelial
cadherin
NM_004360
CDKN2A cyclin-dependent kinase Inhibitor 2A NM_000077
CHEK2 Checkpoint kinase 2 NM_001005735
EPCAM Epithelial cell adhesion molecule NM_002354
MET hepatocyte growth factor receptor NM_000245
MLH1 MutL homolog 1 NM_000249.3
MSH2 MutS homolog 2 NM_000251.2
MSH6 MutS homolog 6 NM_000179.2
MUTYH MutY homolog NM_001128425.1
PMS2 Mismatch repair endonuclease PMS2 NM_000535
PTEN Phosphatase and tensin homolog NM_000314.4
SMAD4 SMAD family member 4 NM_005359.5
STK11 Serine/threonine kinase 11 NM_000455.4
TP53 Tumor protein p53 NM_000546.5
卵巢癌遗传性易感基因检测
基因名 名称及信息描述 NCBI 编码
ATM Ataxia telangiectasia mutated NM_000051.3
BARD1 BRCA1 associated RING domain 1 NM_000465.2
BRCA1 Breast cancer 1, early onset NM_007300.3
BRCA2 Breast cancer 2, early onset NM_000059.3
BRIP1 BRCA1 interacting protein C-terminal
helicase 1
NM_032043.1
CDH1 Cadherin 1, type 1, E-cadherin (epithelial) NM_004360.3
CHEK2 Checkpoint kinase 2 NM_001005735
.1
DIRAS3 DIRAS family, GTP-binding RAS-like 3 NM_004675.2
EPCAM Epithelial cell adhesion molecule NM_002354
ERBB2 Receptor tyrosine-protein kinase erbB-2 NM_001005862
MLH1 MutL homolog 1 NM_000249
MRE11A Double-strand break repair protein MRE11A NM_005590
MSH2 MutS protein homolog 2 NM_000251
MSH6 mutS homolog 6 NM_000179
MUTYH mutY Homolog (E. coli) NM_001048171
NBN Nibrin NM_001024688
NF1 neurofibromatosis-related protein NF-1 NM_000267
PLAB2 Partner and localizer of BRCA2 NM_024675.3
PMS2 Mismatch repair endonuclease PMS2 NM_000535
PTEN Phosphatase and tensin homolog NM_000314.4
RAD50 RAD50 homolog (S. cerevisiae) NM_133482.1
RAD51C RAD51 homolog C (S. cerevisiae) NM_002876
RAD51D DNA repair protein RAD51 homolog 4 NM_001142571
STK11 Serine/threonine kinase 11 NM_000455.4
TP53 Tumor protein p53 NM_001126114
.1
乳腺癌基因检测
基因名 名称及信息描述 NCBI 编码
AR Androgen receptor NM_000044.3
ATM Ataxia telangiectasia mutated NM_000051.3
BARD1 BRCA1 associated RING domain 1 NM_000465.2
BRCA1 Breast cancer 1, early onset NM_007300.3
BRCA2 Breast cancer 2, early onset NM_000059.3
BRIP1 BRCA1 interacting protein C-terminal
helicase 1
NM_032043.1
CDH1 Cadherin 1, type 1, E-cadherin (epithelial) NM_004360.3
CHEK2 Checkpoint kinase 2 NM_001005735
.1
DIRAS3 DIRAS family, GTP-binding RAS-like 3 NM_004675.2
ERBB2/Her
2
v-erb-b2 avian erythroblastic leukemia
viral oncogene homolog 2
NM_004448.2
NBN Nibrin NM_002485.4
PALB2 Partner and localizer of BRCA2 NM_024675.3
PTEN Phosphatase and tensin homolog NM_000314.4
RAD50 RAD50 homolog (S. cerevisiae) NM_133482.1
RAD51 RAD51 recombinase NM_058216.1
STK11 Serine/threonine kinase 11 NM_000455.4
TP53 Tumor protein p53 NM_001126114
.1
CASP8 Caspase 8, apoptosis-related cysteine NM_001080125
peptidase .1
TGFB1 Transforming growth factor, beta 1 NM_000660.3
肿瘤遗传性易感基因(39 Gene)检测
序
号
基因 相关疾病
1 APC 家族性结肠腺瘤息肉病、结直肠癌等
2 ATM 共济失调毛细血管扩张症、淋巴样恶性肿瘤包括淋巴瘤和
白血病、乳腺癌等
3 BARD1 乳腺癌等
4 BMPR1A 结肠癌、患胃癌、胰腺癌等
5 BRCA1 乳腺癌、卵巢癌等
6 BRCA2 乳腺癌、前列腺癌等
7 BRIP1 乳腺癌、卵巢癌等
8 CDH1 胃癌、乳腺癌等
9 CDK4 鼻咽癌、食道癌、乳腺癌等
10 P16(CDKN2A) 黑色素瘤、甲状腺乳头状癌、肝癌、鼻咽癌、胃癌等
11 CHEK2 乳腺癌、食管癌、卵巢癌等
12 ELAC2 前列腺癌等
13 EPCAM 乳腺癌、肝癌、肾癌、膀胱癌等
14 FANCC 胰腺癌、乳腺癌等
15 HRAS1 非恶性黑色素瘤皮肤癌、Costello 综合征等
16 MEN1 肺腺癌、甲状旁腺肿瘤、胰腺及十二指肠神经内分泌肿瘤
和垂体瘤等
17 MET 实体瘤
18 MLH1 口腔癌、甲状腺癌、结直肠癌、子宫内膜癌、胃癌、
Lynch 综合症等
19 MRE11A 膀胱癌、Nijmegen 染色体断裂综合症等
20 MSH2 结直肠癌、子宫内膜癌、胃癌、Lynch 综合症等
21 MSH6 结直肠癌、子宫内膜癌、胃癌等
22 MUTYH 结直肠癌等
23 NBN 乳腺癌、Nijmegen 染色体断裂综合症等
24 NF1 I 型多发性神经纤维瘤、乳腺癌等
25 NTRK1 肺癌、多形性胶质母细胞瘤等
26 PALB2 乳腺癌等
27 PALLD 胰腺癌等
28 PMS2 结直肠癌、子宫内膜癌等
29 PTCH1 胃癌、膀胱癌、鼻咽癌等
30 PTEN
胶质母细胞瘤、前列腺癌、子宫内膜癌、肾癌、卵巢癌、
乳腺癌、肺癌、膀胱癌、甲状腺癌、头颈部鳞状细胞癌、
黑色素瘤、淋巴瘤、Cowden 综合症等
31 RAD50 鼻咽癌、白血病、Nijmegen 染色体断裂综合症等
32 RAD51 头颈部鳞状细胞癌、肺癌、乳腺癌、结直肠癌、膀胱癌等
33 RAD51C 乳腺癌、卵巢癌等
34 RAD51D 卵巢癌和乳腺癌等
35 RET 肺癌、甲状腺癌等
36 SMAD4 结直肠癌、胰腺癌、胃癌等
37 STK11 结直肠癌、肺癌、Peutz Jeghers 综合征等
38 TP53 结直肠癌、鼻咽癌、白血病、卵巢癌、Li-Fraumeni 综合
症等
39 VHL 肾癌、肝癌、结直肠癌、Von Hippel-Lindau 综合征等
肿瘤遗传性易感基因(94 Gene)检测
AIP、ALK、APC、ATM BAP1、BLM、BMPR1A、BRCA1、BRCA2、
BRIP1、BUB1B
CDC73、CDH1、CDK4、CDKN1C、
CDKN2A、CEBPA、CEP57、CHEK2、CYLD
DDB2、DICER1、DIS3L2
EGFR、EPCAM、ERCC2、ERCC3、
ERCC4、ERCC5、EXT1、EXT2、EZH2
FANCA、FANCB、FANCC、FANCD2、
FANCE、FANCF、FANCG、FANCI、
FANCL、FANCM、FH、FLCN
GATA2、GPC3 HNF1A、HRAS
KIT MAX、MEN1、MET、MLH1、MSH2、
MSH6、MUTYH
NBN、NF1、NF2、NSD1 PALB2、PHOX2B、PMS1、PMS2、PRF1、
PRKAR1A、PTCH1、PTEN
RAD51C、RAD51D、RB1、RECQL4、
RET、RHBDF2、RUNX1
SBDS、SDHAF2、SDHB、SDHC、SDHD、
SLX4、SMAD4、SMARCB1、STK11、SUFU
TMEM127、TP53、TSC1、TSC2 VHL
WRN、WT1 XPA、XPC
遗传性耳聋基因检测
序号 基因 遗传方式
1 ACTB
2 ACTG1 常染色体显性遗传 (DFNA)
3 ATP6V1B1 常染色体显性遗传 (DFNA)
4 ATP6V1B2 常染色体显性遗传 (DFNA)
5 BCS1L 常染色体显性遗传 (DFNA)
6 BSND 常染色体隐性遗传 (DFNB)
7 CATSPER2
8 CCDC50 常染色体显性遗传 (DFNA)
9 CDH23 常染色体隐性遗传 (DFNB)
10 CEACAM16 常染色体显性遗传 (DFNA)
11 CLDN14 常染色体隐性遗传 (DFNB)
12 COCH 常染色体显性遗传 (DFNA)
13 COL11A2 常染色体隐性遗传 (DFNB)
14 COL9A2
15 COL9A3
16 CRYM 常染色体显性遗传 (DFNA)
17 DFNA5 常染色体显性遗传 (DFNA)
18 DFNB31 常染色体隐性遗传 (DFNB)
19 DFNB59 常染色体隐性遗传 (DFNB)
20 DIAPH1 常染色体显性遗传 (DFNA)
21 DSPP 常染色体显性遗传 (DFNA)
22 ECE1
23 EDNRA 常染色体显性遗传 (DFNA)
24 EDNRB 常染色体显性遗传 (DFNA)
25 ERCC2 常染色体隐性遗传 (DFNB)
26 ERCC3 常染色体隐性遗传 (DFNB)
27 ESPN 常染色体隐性遗传 (DFNB)
28 ESRRB 常染色体隐性遗传 (DFNB)
29 EYA4 常染色体显性遗传 (DFNA)
30 FAS
31 FGF3
32 FGFR3
33 FOXI1 常染色体隐性遗传 (DFNB)
34 GATA3
35 GIPC3 常染色体隐性遗传 (DFNB)
36 GJA1 常染色体隐性遗传 (DFNB)
37 Gjb1 X 连锁遗传
38 Gjb2 10.6K常染色体隐性遗传,小部分显性
遗传
39 GJB3 常染色体显性遗传 (DFNA)
40 GJB4
41 GJB6常染色体显性遗传,小部分隐性
遗传
42 GPSM2 常染色体隐性遗传 (DFNB)
43 GRHL2 常染色体显性遗传 (DFNA)
44 GRXCR1 常染色体隐性遗传 (DFNB)
45 GSTP1
46 HAL
47 HGF 常染色体隐性遗传 (DFNB)
48 ILDR1 常染色体隐性遗传 (DFNB)
49 JAG1
50 KCNE1 常染色体显性遗传 (DFNA)
51 KCNJ10 常染色体显性遗传 (DFNA)
52 KCNQ1 常染色体显性遗传 (DFNA)
53 KCNQ4 常染色体显性遗传 (DFNA)
54 KIAA1199
55 LHFPL5 常染色体隐性遗传 (DFNB)
56 LHX3
57 LOXHD1 常染色体隐性遗传 (DFNB)
58 LRTOMT 常染色体隐性遗传 (DFNB)
59 MARVELD2 常染色体隐性遗传 (DFNB)
60 mir182
61 mir183
62 mir96 常染色体显性遗传 (DFNA)
63 MITF 常染色体显性遗传 (DFNA)
64 MSRB3 常染色体隐性遗传 (DFNB)
65 MTAP
66 MT-TD 线粒体遗传
67 MT-TH 线粒体遗传
68 MT-TI 线粒体遗传
69 MT-TK 线粒体遗传
70 MT-TL1 线粒体遗传
71 MT-TL2 线粒体遗传
72 MT-TM 线粒体遗传
73 MT-TQ 线粒体遗传
74 MT-TS1 线粒体遗传
75 MT-TS2 线粒体遗传
76 MYH14 常染色体显性遗传 (DFNA)
77 MYH9 常染色体显性遗传 (DFNA)
78 MYO15A 常染色体隐性遗传 (DFNB)
79 MYO1A 常染色体显性遗传 (DFNA)
80 MYO1C
81 MYO1F
82 MYO3A 常染色体隐性遗传 (DFNB)
83 MYO6
84 MYO7A常染色体显性遗传 (DFNA)
或常染色体隐性遗传 (DFNB)
85 NDP X-连锁隐性遗传
86 NR2F1
87 OTOA 常染色体隐性遗传 (DFNB)
88 OTOF 常染色体隐性遗传 (DFNB)
89 OTOR
90 P2RX2 常染色体显性遗传 (DFNA)
91 PAX3 常染色体显性遗传 (DFNA)
92 PCDH15 常染色体显性遗传 (DFNA)
93 PDZD7 常染色体隐性遗传 (DFNB)
94 PMP22
95 POU3F4 X-连锁(DFNX)隐性遗传
96 POU4F3 常染色体显性遗传 (DFNA)
97 PRPS1 X-连锁(DFNX)
98 PTPRQ 常染色体隐性遗传 (DFNB)
99 RDX 常染色体隐性遗传 (DFNB)
100 SERPINB6 常染色体隐性遗传 (DFNB)
101 SIX1 常染色体显性遗传 (DFNA)
102 SIX5 常染色体显性遗传 (DFNA)
103 SLC17A8 常染色体显性遗传 (DFNA)
104 SLC26A4 常染色体隐性遗传 (DFNB)
105 SLC26A5 常染色体隐性遗传 (DFNB)
106 SLC4A11 常染色体显性遗传 (DFNA)
107 SMPX X-连锁(DFNX)
108 SNAI2 常染色体显性遗传 (DFNA)
109 SOX2 常染色体显性遗传
110 SPINK5 常染色体隐性遗传病
111 STRC 常染色体隐性遗传 (DFNB)
112 TBL1X
113 TCF21
114 TECTA常染色体显性遗传,小部分隐性
遗传
115 TFCP2 常染色体显性遗传
116 TIMM8A X 连锁隐性遗传
117 TJP2 常染色体显性遗传 (DFNA)
118 TMC1常染色体隐性遗传,小部分显性
遗传
119 TMIE 常染色体隐性遗传 (DFNB)
120 TMPRSS3 常染色体隐性遗传 (DFNB)
121 TMPRSS5 常染色体隐性遗传 (DFNB)
122 TPRN 常染色体隐性遗传 (DFNB)
123 TRIOBP 常染色体隐性遗传 (DFNB)
124 USH1C-a-b 常染色体隐性遗传 (DFNB)
125 USH1G 常染色体隐性遗传 (DFNB)
126 USH2A 常染色体隐性遗传 (DFNB)
127 USH2C 常染色体隐性遗传 (DFNB)
128 USH3A 常染色体隐性遗传 (DFNB)
129 WFS1 常染色体显性遗传 (DFNA)
健康守护基因检测
序
号相关疾病或药物 基因
1 遗传性乳腺癌-卵巢癌综合征 BRCA1、BRCA2
2 李法美尼综合征 TP53
3 黑斑息肉综合征 STK11
4 林奇综合征 MLH1、MSH2、MSH6、PMS2
5 MYH 相关息肉病 MUTYH
6
VHL 综合征(林道氏综合
征,视网膜和中枢神经血管
母细胞病)
VHL
71 型多发内分泌腺瘤
(MEN1)MEN1
82 型多发内分泌腺瘤
(MEN2)RET
9家族性髓样甲状腺癌
(FMTC)RET、NTRK1
10 1 型家族性腺瘤息肉病/APC APC
11 遗传性弥漫性胃癌 CDH1
12 黑色素瘤-胰腺癌综合征 CDKN2A
13 考登综合征 PTEN
14 幼年性息肉病综合征 BMPR1A、SMAD4
15 痣样基底细胞癌综合征 PTCH
16埃勒斯 - 当洛综合征 - 血
管型COL3A1
17肥厚型心肌病, 扩张型心肌
病
MYBPC3、MYH7、TNNT2、TNNI3、TPM1、
MYL3、ACTC1、PRKAG2、GLA、LMNA、TTN
18儿茶酚胺敏感性多形性室性
心动过速RYR2
19 致心律失常性右室心肌病 PKP2、DSP、DSG2
20
Romano-ward 长 QT 综合征
1、2、3类型,
Brugada 综合症
KCNQ1、KCNH2、SCN5A
21 家族性高胆固醇 LDLR、APOB、PCSK9
22 恶性高热易感性 RYR1
23氨基糖苷类抗生素而导致耳
聋MTRNR1
24 叶酸代谢障碍 (A1555G)
25 凝血因子 V Leiden 突变 MTHFR
26 卡马西平个体化用药 (Rs1801131,rs1801133)
27琥珀胆碱类药物的个体化用
药F5
28 氟氯西林个体化用药 (rs6025)
29 硫嘌呤类药物个体化用药 HLA-B
30 伊立替康个体化用药 (rs2844682, rs3909184)
31 5-氟尿嘧啶个体化用药 BCHE
32 他汀类个体化用药 (rs1799807, rs1803274)
33 辛伐他汀个体化用药 HLA-B
34 华法林的个体化用药( rs2395029)、TPMT、(rs1142345,
rs1800460, rs1800462)
35 氯吡格雷个体化用药 UGT1A1
36β-受体阻滞剂作为心衰治疗
的个体化用药(rs10929302)
高脂血症相关基因检测
序号 基因 相关疾病
1 LPL I型高脂蛋白血症
2 APOC2 Ib型高脂蛋白血症和家族性载脂蛋白C-II缺乏症
3 APOC3 Ib型高脂蛋白血症和家族性载脂蛋白C-III缺乏症
4 ApoE4 III型高脂蛋白血症或家族性血β脂蛋白异常
5 APOA1 低α脂蛋白血症和ApoA1相关的家族性内脏淀粉样变
6 APOA4* 高胆固醇血症慢性炎症性脱髓鞘性多发性神经病
7 LPAⅢ型高脂血症Alagille综合征,家族性高脂血症与动脉粥样
硬化
8 CETP I型高α脂蛋白血症和CETP相关α脂高脂蛋白血症
9 NPC1 C 型尼曼氏病
10 ABCA1 丹吉尔疾病和家族性高密度脂蛋白缺乏
11 LCAT 高胆固醇血症,高α脂蛋白血症和诺卢姆病
12 LIPC 肝脂酶缺乏症和高脂血症
13 ABCG5 谷固醇血症和主动脉动脉粥样硬化
14 ABCG8 谷固醇血症和胆囊疾病
15 LIPA 沃尔曼病沉积病
16 MYLIP β脂蛋白缺乏症
17 ABCG1** 丹吉尔病和谷固醇血症
18 LDLR 家族性高胆固醇血症和ldlr相关家族性高胆固醇血症
19 APOB 低β脂蛋白血症和高胆固醇血症
20 PCSK9 家族性高胆固醇血症
21 APOC4 冠心病和冠状动脉疾病
22 APOA5*** 高甘油三酯血症和5型高脂蛋白血症
人类线粒体基因组检测
mtDNA 编码 rRNA(2 个基因),tRNA(22 个基因)和 13 个参与呼吸链的部
分蛋白质。线粒体是真核细胞的“动力工厂”。人类线粒体基因组仅有 16,569
个碱基对。其中,与线粒体突变相关的临床疾病名单如下:
成人
神经系统:偏头痛,中风,癫痫,痴呆,肌病,周围神经病变,复视,共
济失调,言语障碍,感觉神经性耳聋
胃肠道:便秘,肠易激,语言障碍
心脏:心力衰竭,心脏阻塞,心肌病
呼吸:呼吸衰竭,夜间通气不畅,反复抽吸,肺炎
内分泌:糖尿病,甲状腺疾病,甲状旁腺疾病,卵巢功能衰竭
眼科:视神经萎缩,白内障,眼肌麻痹,上睑下垂
儿科
神经病学:癫痫,肌病,精神运动迟缓,共济失调,痉挛,肌张力障碍,
感音性耳聋
胃肠道:呕吐,发育不良,功能障碍
心脏:心室肥厚性心肌病, 心律失常
呼吸:中枢通气不畅,呼吸暂停
血液学:贫血,全血细胞减少
肾脏: 肾小管畸形
肝脏:肝衰竭
内分泌:糖尿病,肾上腺衰竭
眼科:视神经萎缩
人类遗传性疾病基因(4503 基因) 检测
Disease No. of Genes on Panel
Autism Spectrum Disorders 60
Cardiomyopathy 93
Arrhythmias 29
Arrhythmogenic Right Ventricular
Dysplasia/Cardiomyopathy
7
Brugada Syndrome 8
Dilated Cardiomyopathy 25
Hypertropic Cardiomyopathy 14
Long and Short QT Syndrome 12
Pulmonary Arterial Hypertension 4
Sudden Cardiac Arrest 10
Thoracic Aortic Aneurysm &
Dissection and Related Disorders
6
Ciliopathies 112
Congenital Disorders of
Glycosylation
66
Congenital Myasthenic Syndromes 11
Epilepsy and Seizure Disorders 108
Eye Disorders 205
Achromatopsia, Cone, and Cone-Rod
Dystrophy
36
Albinism 5
Anophthalmia/Microphthalmia/Anterior
Segment Dysgenesis/Anomaly
22
Bardet-Biedl Syndrome 18
Congenital Stationary Night 15
Blindness
Flecked-Retina Disorders 6
Joubert Syndrome 18
Leber Congenital Amaurosis 18
Macular
Dystrophy/Degeneration/Stargardt
Disease
16
Neuronal Ceroid Lipofuscinoses 11
Optic Atrophy 5
Retinitis Pigmentosa 65
Senior Loken Syndrome 7
Stickler Syndrome 5
Usher Syndrome 13
Vitreoretinopathy 9
Comprehensive Glycogen Storage
Disorders
20
Glycogen Storage Disorders: Liver 11
Glycogen Storage Disorders: Muscle 12
Hearing Loss 87
Hereditary Cancer Syndrome 46
Hereditary Periodic Fever Syndromes 7
Inflammatory Bowel Disease 22
Lysosomal Storage Disorders 55
Maturity Onset Diabetes of the Young 4
Multiple Epiphyseal Dysplasia 7
Neuromuscular Disorders 46
Congenital Muscular Dystrophy 18
Limb-Girdle Muscular Dystrophy 26
Noonan Syndrome and Related
Disorders
12
Peroxisome Biogenesis Disorders,
Zellweger Syndrome Spectrum
15
Short Stature Panel 40
Skeletal Dysplasia 162
X-Linked Intellectual Disability 92
Total 1721
人类遗传性耳聋基因热点检测
(High Frequency Deafness related SNPs Panel)
Gjb2-35delG
SLC26A4-IVS7-2
A/G 12SrRNA-1555A/G
SLC26A4-
1520delT
Gjb2- 167delT SLC26A4-1174A/T 12SrRNA-1494C/T SLC26A4-1336C>T
Gjb2- 176-
19ldel16 SLC26A4-1226G/A Gjb2-257C/T
SLC26A4-
ivs13+9C>T
Gjb2-235DelC SLC26A4-1229C/T Gjb2_512insAACG SLC26A4-1586T>G
Gjb2-299-
300delAT
SLC26A4-
IVS15+5G/A Gjb2_380G/A SLC26A4-281C>T
Gjb3-538C/T SLC26A4-1975G/C 12SrRNA-1095T/C SLC26A4-946G>T
Gjb3-547G/A SLC26A4-2027T/A 12SrRNA-1116A/G SLC26A4-1991C>T
SLC26A4- 589G/A SLC26A4-2162C/T 12SrRNA-1005T/C
SLC26A4-1687-
1692insA
SLC26A4-2168A/G SLC26A4-235C>T
人扩张型心肌病靶基因检测
序号 基因 蛋白产物
1 ABCC9
ATP-binding cassette,
subfamily c, member 9
2 ACTC Actin, alpha, cardiac muscle
3 ACTN2 Actinin, alpha-2
4 DES Desmin
5 LAMA4 Laminin, alpha-4
6 LDB3 Lim domain-binding 3
7 LMNA Lamin a/c
8 MYBPC3
Myosin-binding protein c,
cardiac
9 MYH6
Myosin, heavy chain 6, cardiac
muscle, alpha
10 MYH7
Myosin, heavy chain 7, cardiac
muscle, beta
11 MYPN
Myopalladin PLN Sarcoplasmic
reticulum Phospholamban
12 PLN Phospholamban
13 PSEN1 Presenilin 1
14 PSEN2 Presenilin 2
15 RBM20 RNA-binding motif protein 20
16 SCN5A Sodium channel
17 SGCD Sarcoglycan, delta
18 TAZ/G4.5 Tafazzin
19 TCAP Titin-cap
20 TMPO Thymopoietin
21 TNNI3 Cardiac troponin i
22 TNNT2 Troponin t2, cardiac
23 TPM1 Tropomyosin 1
24 VCL Vinculin
25 MTTD
Mitochondrial transfer RNA
aspartic acid
26 MTTH
Mitochondrial transfer RNA
histidine
27 MTTINC
Mitochondrial transfer RNA
isoleucine
28 MTTK
Mitochondrial transfer RNA
lysine
29 MTTL1
Mitochondrial transfer RNA
leucine
30 MTTL2
Mitochondrial transfer RNA
leucine
31 MTTM
Mitochondrial transfer RNA
methionine
32 MTTQ
Mitochondrial transfer RNA
glutamine
33 MTTS1
Mitochondrial transfer RNA
serinel
34 MTTS2
Mitochondrial transfer RNA
leucine2
人肥厚型心肌病靶基因检测
序号 基因 蛋白产物
1 ACTC1 Cardiac actin 1
2 BMPR2
Bone morphogenetic protein
receptor type II
3 CAV3
Caveolin 3 (Muscular
dystrophy)
4 GLA
Galactosidase alpha (Fabry
disease) –
5 LAMP2
Lysosome-associated membrane
protein 2
6 MYBPC3
Cardiac myosin-binding
protein C
7 MYH7 ß - Myosin heavy chain
8 MYL2
Regulatory myosin light chain
2
9 MYL3
Essential myosin light chain
3
10 PRKAG2
Noncatalytic AMP-activated
protein kinase gamma 2
11 TNNC1 Troponin C
12 TNNI3 Cardiac troponin I
13 TNNT2 Cardiac troponin T
14 TPM1 Tropomyosin 1
15 TTR Transthyretin (Amyloidosis)
16 MTTG
Mitochondrial transfer RNA
glycine
17 MTTI
Mitochondrial transfer RNA
isoleucine
18 MTTK
Mitochondrial transfer RNA
lysine
19 MTIQ
Mitochondrial transfer RNA
glutamine
PGX™药物基因组学基因检测
ABCB1, ABCG2, ADRA2A, ADRB1, AGT, CACNA1C, CES1, CFTR
COMT, CYP1A2, CYP2C19, CYP2C9, CYP2D6, CYP3A4, CYP3A5
DPYD, DRD1, DRD2, DRD3, EDN1, F2, F5, GNB3, GRIK1, GSTA1
HTR1A, HTR2A, HTR2C, IFNL3, KCNIP1, LDLR, MTHFR,
NAT1, NR1H3, OPRM1, RYR1, SLC6A2, SLCO1B1, TPMT,
UGT2B10, UGT2B7 , VKORC