DBP D-box binding PAR bZIP transcription factor
Information
- Symbol
- DBP
- Type
- protein-coding
- Description
- D-box binding PAR bZIP transcription factor
- Entrez Gene ID
- 1628
- Genome
- hg19
- Position
- chr19:49,133,287-49,140,636
- Genome
- hg38
- Position
- chr19:48,630,030-48,637,379
- MIM
- 124097 OMIM
- HGNC
- HGNC:2697 HGNC
- Ensembl
- ENSG00000105516 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 2 |
| Likely benign | 0 | 6 |
| Uncertain significance | 0 | 30 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
38 |
 |
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 | DABP |
| SYNONYM | taxREB302 |
| MIM | 124097 OMIM |
| HGNC | HGNC:2697 HGNC |
| Ensembl | ENSG00000105516 Ensembl |
| AllianceGenome | HGNC:2697 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000222122.10 | hg38 | chr19 | 48,630,030 | 48,637,379 | 7,350 |
| ENST00000601104.1 | hg38 | chr19 | 48,633,086 | 48,637,363 | 4,278 |
| ENST00000599385.5 | hg38 | chr19 | 48,630,685 | 48,634,636 | 3,952 |
| ENST00000593500.1 | hg38 | chr19 | 48,630,731 | 48,634,526 | 3,796 |
| ENST00000222122.10 | hg19 | chr19 | 49,133,287 | 49,140,636 | 7,350 |
| ENST00000599385.5 | hg19 | chr19 | 49,133,942 | 49,137,893 | 3,952 |
| ENST00000593500.1 | hg19 | chr19 | 49,133,988 | 49,137,783 | 3,796 |
| ENST00000601104.1 | hg19 | chr19 | 49,136,343 | 49,140,620 | 4,278 |
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