TARID TCF21 antisense RNA inducing promoter demethylation
Information
- Symbol
- TARID
- Type
- ncRNA
- Description
- TCF21 antisense RNA inducing promoter demethylation
- Entrez Gene ID
- 100507308
- Genome
- hg19
- Position
- chr6:134,205,860-134,213,940
- Genome
- hg38
- Position
- chr6:133,884,722-133,892,802
- MIM
- 616058 OMIM
- HGNC
- HGNC:50506 HGNC
- Ensembl
- ENSG00000227954 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
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0 |
 |
0 |
 |
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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| 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 | EYA4-AS1 |
| MIM | 616058 OMIM |
| HGNC | HGNC:50506 HGNC |
| Ensembl | ENSG00000227954 Ensembl |
| AllianceGenome | HGNC:50506 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000630119.2 | hg38 | chr6 | 133,884,722 | 133,892,802 | 8,081 |
| ENST00000607033.5 | hg38 | chr6 | 133,502,252 | 133,888,982 | 386,731 |
| ENST00000607033.5 | hg19 | chr6 | 133,823,390 | 134,210,120 | 386,731 |
| ENST00000630119.2 | hg19 | chr6 | 134,205,860 | 134,213,940 | 8,081 |
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