使用本网站需要启用 JavaScript, 请启用后刷新页面获得更好的体验
登录
注册
首页
个人基因检测
临床应用研究
科研合作项目
合作与服务
社区
研究所
微解读
应用
姓氏祖源
基因关系
原始数据
使用 WeGene 需要启用 Cookies, 请启用后刷新页面获得更好的体验
社区首页
小组
Usher 综合征
Usher 综合征
发起讨论
Usher 综合征
11 个讨论
只看精华帖
按热门排序
按最新排序
RS397518039是什么点位啊
hulihuli
• 3 天前
50
0
• 来自相关小组
chr1:215844567是什么位点？
xuebowen021
• 最后回复
唏嘘的8号染色体
•
2021-11-28 12:19
2108
1
• 来自相关小组
我天生夜盲，耳朵对低音讲话的人辨识度有点差。。
热血豆腐
• 最后回复
xuebowen021
•
2021-11-28 06:07
2354
2
• 来自相关小组
携带usher综合征基因
咆哮的GCFC2基因
• 最后回复
zhengqiang
•
2021-04-08 00:41
1711
1
• 来自相关小组
求助，夫妻双方都是usher综合症风险变异携带者，产前怎么办？
养猫的17号染色体
• 最后回复
AileenJS
•
2019-06-04 23:06
4426
6
• 来自相关小组
我是不是别找也携带的人生孩子就风险不大？
狗酱酱
• 最后回复
mabaoyuan037
•
2019-03-13 18:45
2260
2
• 来自相关小组
这个是隐性疾病，有携带是不是没关系啊？
Jamie杰
• 最后回复
虚心的GOT2基因
•
2018-12-27 16:46
2503
1
• 来自相关小组
携带一个基因间突变
摩羯的RXRA基因
• 2018-12-16 07:29
2350
0
• 来自相关小组
有这个是不是不要小孩比较好啊
俊逸的MLH1基因
• 最后回复
俊逸的MLH1基因
•
2018-12-13 21:25
2622
3
• 来自相关小组
这是啥？需不需要去医院查查啊
伤情的DSCAM基因
• 最后回复
hahadada
•
2018-12-12 19:36
2652
3
• 来自相关小组
卧槽 我确实感觉自己耳背
黑豆浆2333
• 最后回复
元月十号
•
2018-12-09 11:12
2403
1
• 来自相关小组
发起讨论
Usher 综合征
11 个讨论
相关基因
MYO7A
位点：RS111033174
位点：RS111033178
位点：RS111033180
位点：RS111033181
位点：RS111033182
位点：RS111033192
位点：RS111033198
位点：RS111033201
位点：RS111033206
位点：RS111033214
位点：RS111033233
位点：RS111033283
位点：RS111033285
位点：RS111033290
位点：RS111033389
位点：RS111033426
位点：RS111033482
位点：RS121965079
位点：RS121965085
位点：RS199606180
位点：RS28934610
位点：RS35689081
位点：RS397516281
位点：RS397516283
位点：RS397516284
位点：RS397516291
位点：RS397516295
位点：RS397516301
位点：RS397516310
位点：RS397516312
位点：RS397516315
位点：RS397516317
位点：RS397516320
位点：RS397516321
位点：RS397516322
位点：RS397516323
位点：RS397516324
位点：RS397516331
位点：RS397516332
位点：RS41298133
位点：RS797044518
位点：RS782252317
位点：RS781811444
位点：RS797044491
位点：RS797044511
位点：RS201892914
位点：RS781988557
位点：RS376535635
位点：RS199897298
位点：RS117966637
位点：RS369458838
位点：RS727503329
位点：RS397516316
位点：RS727504541
位点：RS111033215
位点：RS773844428
位点：RS377670513
位点：RS878853236
位点：RS878864531
CLRN1
位点：RS111033258
位点：RS111033267
位点：RS111033434
位点：RS121908140
位点：RS121908141
位点：RS121908143
位点：RS374963432
位点：RS201008540
PCDH15
位点：RS111033260
位点：RS137853001
位点：RS202033121
位点：RS397517452
位点：RS727504301
USH2A
位点：RS111033264
位点：RS111033265
位点：RS111033272
位点：RS111033273
位点：RS111033334
位点：RS111033364
位点：RS111033382
位点：RS111033385
位点：RS111033414
位点：RS111033417
位点：RS111033418
位点：RS111033526
位点：RS121912599
位点：RS121912600
位点：RS202175091
位点：RS369522997
位点：RS397517974
位点：RS397517976
位点：RS397517977
位点：RS397517979
位点：RS397517988
位点：RS397517989
位点：RS397517990
位点：RS397517994
位点：RS397518021
位点：RS397518022
位点：RS397518023
位点：RS397518026
位点：RS397518029
位点：RS397518036
位点：RS397518041
位点：RS397518042
位点：RS397518046
位点：RS397518048
位点：RS398124619
位点：RS41308425
位点：RS483353056
位点：RS527236137
位点：RS527236139
位点：RS80338904
位点：RS146733615
位点：RS727504867
位点：RS753330544
位点：RS201238640
位点：RS727505337
位点：RS727504608
位点：RS372347027
位点：RS201657446
位点：RS794727579
位点：RS727503725
位点：RS727503731
位点：RS797045113
位点：RS794729204
位点：RS727503736
位点：RS397517963
位点：RS111033280
位点：W01216380743
CDH23
位点：RS111033270
位点：RS183431253
位点：RS367928692
位点：RS370983472
位点：RS397517323
位点：RS397517326
位点：RS397517327
位点：RS397517329
位点：RS397517337
位点：RS397517341
位点：RS397517342
位点：RS397517346
位点：RS397517353
位点：RS397517354
位点：RS397517362
位点：RS727502931
位点：RS140884994
USH1C
位点：RS121908370
位点：RS151045328
位点：RS138138689
位点：RS377145777
ADGRV1
位点：RS121909762
位点：RS371981035
位点：RS373780305
位点：RS397517436
USH1G
位点：RS397517925
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 8
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 7
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 9
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 3.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 5
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 10
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 4
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutations in the VLGR1 gene implicate G-protein signaling in the pathogenesis of Usher syndrome type II.
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
Usher syndrome type I G (USH1G) is caused by mutations in the gene encoding SANS, a protein that associates with the USH1C protein, harmonin.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutation of CDH23, encoding a new member of the cadherin gene family, causes Usher syndrome type 1D.
Mutations in a novel gene with transmembrane domains underlie Usher syndrome type 6
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Defective myosin VIIA gene responsible for Usher syndrome type 1B.
Mutations of the protocadherin gene PCDH15 cause Usher syndrome type 1F.
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
Mutation of a gene encoding a protein with extracellular matrix motifs in Usher syndrome type IIa.
深圳市市场监督管理局企业主体身份公示
中文
English