TAF11 TATA-box binding protein associated factor 11
Information
- Symbol
- TAF11
- Type
- protein-coding
- Description
- TATA-box binding protein associated factor 11
- Entrez Gene ID
- 6882
- Genome
- hg19
- Position
- chr6:34,845,239-34,855,819
- Genome
- hg38
- Position
- chr6:34,877,462-34,888,042
- MIM
- 600772 OMIM
- HGNC
- HGNC:11544 HGNC
- Ensembl
- ENSG00000064995 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 | MGC:15243 |
| SYNONYM | PRO2134 |
| SYNONYM | TAF2I |
| SYNONYM | TAFII28 |
| MIM | 600772 OMIM |
| HGNC | HGNC:11544 HGNC |
| Ensembl | ENSG00000064995 Ensembl |
| AllianceGenome | HGNC:11544 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000686190.1 | hg38 | chr6 | 34,878,129 | 34,887,957 | 9,829 |
| ENST00000650109.1 | hg38 | chr6 | 34,877,462 | 34,888,027 | 10,566 |
| ENST00000361288.9 | hg38 | chr6 | 34,877,462 | 34,888,042 | 10,581 |
| ENST00000420584.3 | hg38 | chr6 | 34,877,778 | 34,888,071 | 10,294 |
| ENST00000650109.1 | hg19 | chr6 | 34,845,239 | 34,855,804 | 10,566 |
| ENST00000361288.9 | hg19 | chr6 | 34,845,239 | 34,855,819 | 10,581 |
| ENST00000420584.3 | hg19 | chr6 | 34,845,555 | 34,855,848 | 10,294 |
| ENST00000686190.1 | hg19 | chr6 | 34,845,906 | 34,855,734 | 9,829 |
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