About Mitofam
Add Pedigree
Help
About Mitofam
Add Pedigree
Help
MT-RNR1&2
A2755G
A2755G-F1
C2639A
C3093G
C3093G-F1
G2492A
G2647A
G3010A
G3054A
G3090A
T2336C
T2336C-F1
T2648C
T2806A
T3098C
A735G
A735G-F2
A735G-F1
A745G
A747G
A801G
A856G
A1027G
A1331G
A1374G
A1453G
A1517C
A1555G
A1555G-F9
A1555G-F10
A1555G-F11
A1555G-F353
A1555G-F323
A1555G-F302
A1555G-F228
A1555G-F227
A1555G-F186
A1555G-F185
A1555G-F226
A1555G-F183
A1555G-F112
A1555G-F182
A1555G-F225
A1555G-F111
A1555G-F66
A1555G-F181
A1555G-F110
A1555G-F65
A1555G-F136
A1555G-F222
A1555G-F109
A1555G-F63
A1555G-F120
A1555G-F133
A1555G-F102
A1555G-F108
A1555G-F61
A1555G-F119
A1555G-F125
A1555G-F70
A1555G-F2
A1555G-F221
A1555G-F58
A1555G-F100
A1555G-F107
A1555G-F1
A1555G-F24
A1555G-F118
A1555G-F124
A1555G-F56
A1555G-F69
A1555G-F23
A1555G-F81
A1555G-F55
A1555G-F99
A1555G-F106
A1555G-F22
A1555G-F7
A1555G-F116
A1555G-F123
A1555G-F53
A1555G-F21
A1555G-F68
A1555G-F80
A1555G-F4
A1555G-F220
A1555G-F83
A1555G-F95
A1555G-F32
A1555G-F98
A1555G-F104
A1555G-F20
A1555G-F31
A1555G-F12
A1555G-F114
A1555G-F27
A1555G-F122
A1555G-F29
A1555G-F26
A1555G-F67
A1555G-F28
A1555G-F71
A1555G-F82
A1555G-F92
A1555G-F93
A1555G-F96
A1555G-F97
A1555G-F103
A1555G-F113
A1555G-F121
C792T
C869T
C1192A
C1192T
C1226G
C1310T
C1494T
C1494T-F11
C1494T-F10
C1494T-F9
C1494T-F8
C1494T-F7
C1494T-F6
C1494T-F5
C1494T-F4
C1494T-F3
C1494T-F2
C1494T-F1
C1537T
C1556T
G988A
T669C
T669C-F2
T721C
T850C
T921C
T961G
T961G-F2
T990C
T1180G
T1391C
T1413C
T1452C
A839G
Edit by Mitofam Team
-
+
首页
A1555G-F83
**Figure 1\. Pedigree diagram for family A1555G\-F83\.**  # Pedigree Information | **No.** | **Position** | **Variant** | **Family ID** | **Nationality** | **Diseases** | **Unaffected Maternal Relatives** | **Affected Maternal Relatives** | **Publication Year** | **PMID/Ref** | **Note** | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 1 | 1555 | m.1555A\>G | A1555G\-F83 | Poland | Aminoglycoside\-induced sensorineural hearing loss | 0 | 1 | 2002 | [11857751](https://pubmed.ncbi.nlm.nih.gov/11857751/) | | The **m.1555A\>G** variant in MT\-RNR1 was reported in family A1555G\-F83 from Poland with aminoglycoside\-induced sensorineural hearing loss. The pedigree record reported 0 unaffected and 1 affected maternal relatives, and the carrier table includes 2 listed carriers. Homoplasmy was reported in all listed carriers; 2/2 carriers were affected, and the main clinical manifestation among affected carriers was severe hearing impairment. # Carrier Information | **No.** | **Position** | **Variant** | **Family ID** | **Carrier ID** | **Type (Fam/De novo/Uninf)** | **Gender (F/M)** | **Proband (Y/N)** | **Affected (Y/N)** | **Die/Alive(D/A)** | **Age** | **Blood Mutant Level** | **Muscle Mutant level** | **Urine Mutant level** | **Other Mutant level** | **Clinical Features** | **Note** | | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | --- | | 1 | 1555 | m.1555A\>G | A1555G\-F83 | A1555G\-F83\-I1 | Uninf | F | ND | Y | ND | ND | Homo | / | / | / | Severe hearing impairment | Gentamicin exposure; after gentamycin exposure | | 2 | 1555 | m.1555A\>G | A1555G\-F83 | A1555G\-F83\-I2 | Uninf | F | ND | Y | ND | ND | Homo | / | / | / | Severe hearing impairment | Gentamicin exposure; after gentamycin exposure | For abbreviations and other usage instructions, please see [Mitofam Info](https://mitofam.com/doc/385/).
Haoying Chen
2026年7月1日 02:25
转发
收藏文档
上一篇
下一篇
手机扫码
复制链接
手机扫一扫转发分享
复制链接
分享
链接
类型
密码
更新密码
有效期
Markdown文件
Word文件
PDF文档
PDF文档(打印)