TGFB1I1 transforming growth factor beta 1 induced transcript 1
Information
- Symbol
- TGFB1I1
- Type
- protein-coding
- Description
- transforming growth factor beta 1 induced transcript 1
- Entrez Gene ID
- 7041
- Genome
- hg19
- Position
- chr16:31,483,473-31,489,279
- Genome
- hg38
- Position
- chr16:31,472,152-31,477,958
- MIM
- 602353 OMIM
- HGNC
- HGNC:11767 HGNC
- Ensembl
- ENSG00000140682 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 66 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
66 |
 |
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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| 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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| 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 | ARA55 |
| SYNONYM | HIC-5 |
| SYNONYM | HIC5 |
| SYNONYM | TSC-5 |
| MIM | 602353 OMIM |
| HGNC | HGNC:11767 HGNC |
| Ensembl | ENSG00000140682 Ensembl |
| AllianceGenome | HGNC:11767 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000567607.5 | hg38 | chr16 | 31,473,426 | 31,477,958 | 4,533 |
| ENST00000394863.8 | hg38 | chr16 | 31,472,152 | 31,477,958 | 5,807 |
| ENST00000394858.6 | hg38 | chr16 | 31,473,205 | 31,477,960 | 4,756 |
| ENST00000361773.7 | hg38 | chr16 | 31,472,208 | 31,477,960 | 5,753 |
| ENST00000394863.8 | hg19 | chr16 | 31,483,473 | 31,489,279 | 5,807 |
| ENST00000394858.6 | hg19 | chr16 | 31,484,526 | 31,489,281 | 4,756 |
| ENST00000361773.7 | hg19 | chr16 | 31,483,529 | 31,489,281 | 5,753 |
| ENST00000567607.5 | hg19 | chr16 | 31,484,747 | 31,489,279 | 4,533 |
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