TFB2M transcription factor B2, mitochondrial
Information
- Symbol
- TFB2M
- Type
- protein-coding
- Description
- transcription factor B2, mitochondrial
- Entrez Gene ID
- 64216
- Genome
- hg19
- Position
- chr1:246,703,863-246,729,563
- Genome
- hg38
- Position
- chr1:246,540,561-246,566,261
- MIM
- 607055 OMIM
- HGNC
- HGNC:18559 HGNC
- Ensembl
- ENSG00000162851 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 14 |
| not provided | 1 | 0 |
| Uncertain significance | 0 | 42 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
60 |
 |
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
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 | Hkp1 |
| SYNONYM | h-mtTFB |
| SYNONYM | h-mtTFB2 |
| SYNONYM | hTFB2M |
| SYNONYM | mtTFB2 |
| MIM | 607055 OMIM |
| HGNC | HGNC:18559 HGNC |
| Ensembl | ENSG00000162851 Ensembl |
| AllianceGenome | HGNC:18559 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000366514.5 | hg38 | chr1 | 246,540,561 | 246,566,261 | 25,701 |
| ENST00000366514.5 | hg19 | chr1 | 246,703,863 | 246,729,563 | 25,701 |
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