TIMM10B translocase of inner mitochondrial membrane 10B
Information
- Symbol
- TIMM10B
- Type
- protein-coding
- Description
- translocase of inner mitochondrial membrane 10B
- Entrez Gene ID
- 26515
- Genome
- hg19
- Position
- chr11:6,502,731-6,505,911
- Genome
- hg38
- Position
- chr11:6,481,501-6,484,681
- MIM
- 607388 OMIM
- HGNC
- HGNC:4022 HGNC
- Ensembl
- ENSG00000132286 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 10 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
10 |
 |
0 |
Frequency
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
EXAC_EAS
EXAC_EAS
HGVD
HGVD
TOMMO
TOMMO
Gene
Position
Disease area statistics
[No Data.]
Locus Zoom
Variants
Search Word
| Target data | : |
MGeND data only
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | FXC1 |
| SYNONYM | TIM10B |
| SYNONYM | Tim9b |
| MIM | 607388 OMIM |
| HGNC | HGNC:4022 HGNC |
| Ensembl | ENSG00000132286 Ensembl |
| AllianceGenome | HGNC:4022 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000254616.11 | hg38 | chr11 | 6,481,501 | 6,484,681 | 3,181 |
| ENST00000530751.1 | hg38 | chr11 | 6,481,501 | 6,482,798 | 1,298 |
| ENST00000530751.1 | hg19 | chr11 | 6,502,731 | 6,504,028 | 1,298 |
| ENST00000254616.11 | hg19 | chr11 | 6,502,731 | 6,505,911 | 3,181 |
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