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小组
Usher 综合征
Usher 综合征
发起讨论
Usher 综合征
8 个讨论
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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
热情的ARX基因
•
2019-07-03 10:32
821
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
1736
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
739
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
1228
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
1030
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
1343
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
1176
3
• 来自相关小组
卧槽 我确实感觉自己耳背
谢泰彤
• 最后回复
元月十号
•
2018-12-09 11:12
970
1
• 来自相关小组
发起讨论
Usher 综合征
8 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：RS111033198
位点：RS111033201
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：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：RS201892914
位点：RS369458838
位点：RS397516316
位点：RS111033215
位点：RS377670513
CLRN1
位点：RS111033258
位点：RS111033267
位点：RS111033434
位点：RS121908140
位点：RS121908141
位点：RS121908143
位点：RS374963432
PCDH15
位点：RS111033260
位点：RS137853001
位点：RS202033121
位点：RS397517452
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：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：RS41308425
位点：RS80338904
位点：RS146733615
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
USH1C
位点：RS121908370
位点：RS151045328
位点：RS138138689
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.
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.
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.
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.
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.
A defect in harmonin, a PDZ domain-containing protein expressed in the inner ear sensory hair cells, underlies Usher syndrome type 1C.
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纯合片段分析
姓氏祖源
祖源平均脸
基因关系
基因保险助手
原始数据
