TBRG4 transforming growth factor beta regulator 4
Information
- Symbol
- TBRG4
- Type
- protein-coding
- Description
- transforming growth factor beta regulator 4
- Entrez Gene ID
- 9238
- Genome
- hg19
- Position
- chr7:45,139,699-45,151,296
- Genome
- hg38
- Position
- chr7:45,100,100-45,111,697
- MIM
- 611325 OMIM
- HGNC
- HGNC:17443 HGNC
- Ensembl
- ENSG00000136270 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 4 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 60 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
68 |
 |
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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| 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 | CPR2 |
| SYNONYM | FASTKD4 |
| MIM | 611325 OMIM |
| HGNC | HGNC:17443 HGNC |
| Ensembl | ENSG00000136270 Ensembl |
| AllianceGenome | HGNC:17443 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000361278.7 | hg38 | chr7 | 45,100,100 | 45,111,718 | 11,619 |
| ENST00000395655.8 | hg38 | chr7 | 45,100,100 | 45,112,047 | 11,948 |
| ENST00000258770.8 | hg38 | chr7 | 45,100,100 | 45,111,697 | 11,598 |
| ENST00000494076.5 | hg38 | chr7 | 45,100,101 | 45,111,706 | 11,606 |
| ENST00000258770.8 | hg19 | chr7 | 45,139,699 | 45,151,296 | 11,598 |
| ENST00000361278.7 | hg19 | chr7 | 45,139,699 | 45,151,317 | 11,619 |
| ENST00000395655.8 | hg19 | chr7 | 45,139,699 | 45,151,646 | 11,948 |
| ENST00000494076.5 | hg19 | chr7 | 45,139,700 | 45,151,305 | 11,606 |
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