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常染色体隐性遗传性非综合征型耳聋
小组 (全基因组常染色体隐性遗传性非综合征型耳聋) 已与当前小组合并
常染色体隐性遗传性非综合征型耳聋
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常染色体隐性遗传性非综合征型耳聋
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能不能更新一下疾病数据库？
zyqhlq
• 最后回复
基因心片海鹏奏
•
2023-10-09 10:06
3364
8
• 来自相关小组
GJB2基因 c.235delC对应哪个rs点位？
leiz05
• 最后回复
冷静的MYT1L基因
•
2021-01-15 09:54
3809
4
• 来自相关小组
我携带多个风险突变耳聋？意味着什么？
蓄须的CFTR基因
• 最后回复
zhengqiang
•
2019-02-20 13:34
3668
3
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常染色体隐性遗传性非综合征型耳聋 携带 1 个风险突变
努力的ABCC1基因
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微胖的EYS基因
•
2019-02-19 19:31
4746
2
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报告当中没有写具体哪个位点变异
猕猴桃含有
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zhengqiang
•
2019-01-18 00:16
3149
2
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发起讨论
常染色体隐性遗传性非综合征型耳聋
5 个讨论
相关基因
GJB2
位点：RS104894395
位点：RS104894409
位点：RS111033190
位点：RS111033203
位点：RS111033217
位点：RS111033294
位点：RS111033420
位点：RS111033451
位点：RS1801002
位点：RS28931592
位点：RS28931595
位点：RS80338949
位点：RS727504302
位点：RS772264564
位点：RS773528125
位点：RS781534323
SLC26A4
位点：RS111033318
位点：RS121908363
位点：RS200455203
OTOF
位点：RS111033330
位点：RS111033341
位点：RS111033342
位点：RS111033373
位点：RS111033383
位点：RS111033447
位点：RS143939430
位点：RS368790049
位点：RS370609551
位点：RS397515582
位点：RS397515584
位点：RS397515586
位点：RS397515605
位点：RS397515608
位点：RS80356584
位点：RS80356589
位点：RS80356597
位点：RS80356599
位点：RS80356604
位点：RS111033349
位点：RS200147906
位点：RS370132645
位点：RS727504936
MARVELD2
位点：RS118203957
TMC1
位点：RS121908073
位点：RS121908074
位点：RS151001642
位点：RS370088722
位点：RS367924428
位点：RS138527651
位点：RS730880359
ESRRB
位点：RS121909110
位点：RS121909111
位点：RS727503041
USH1C
位点：RS146451547
MYO3A
位点：RS193919333
位点：RS199541460
TMIE
位点：RS267607120
位点：RS28941781
位点：RS28942096
位点：RS28942097
位点：RS397517865
位点：RS397517866
MYO7A
位点：RS387906700
PNPT1
位点：RS397514599
MYO15A
位点：RS397517286
位点：RS375290498
位点：RS397517285
位点：RS377015931
位点：RS546575046
CDH23
位点：RS763721044
COL11A2
位点：RS606231410
COL4A4
位点：RS142093416
LOXHD1
位点：RS373937326
位点：RS727505104
MET
位点：RS794728016
MYO6
位点：RS727503326
OTOA
位点：RS148690740
STRC
位点：RS2920791
位点：RS199839039
TRIOBP
位点：RS370737996
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB31
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Usher syndrome 1D and nonsyndromic autosomal recessive deafness DFNB12 are caused by allelic mutations of the novel cadherin-like gene CDH23.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
From flies' eyes to our ears: mutations in a human class III myosin cause progressive nonsyndromic hearing loss DFNB30.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
A mutation in OTOF, encoding otoferlin, a FER-1-like protein, causes DFNB9, a nonsyndromic form of deafness.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Dominant and recessive deafness caused by mutations of a novel gene, TMC1, required for cochlear hair-cell function.
Genomic Landscape and Mutational Signatures of Deafness-Associated Genes
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
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