B3GAT1-DT B3GAT1 divergent transcript
Information
- Symbol
- B3GAT1-DT
- Type
- ncRNA
- Description
- B3GAT1 divergent transcript
- Entrez Gene ID
- 283177
- Genome
- hg19
- Position
- chr11:134,336,079-134,357,809
- Genome
- hg38
- Position
- chr11:134,466,185-134,487,915
- HGNC
- HGNC:27449 HGNC
- Ensembl
- ENSG00000255545 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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 | |||||
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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 | |||
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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 | |||
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Entry | Origin | Type | Annotation |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000531319.2 | hg38 | chr11 | 134,436,473 | 134,505,659 | 69,187 |
ENST00000528482.6 | hg38 | chr11 | 134,466,185 | 134,487,915 | 21,731 |
ENST00000533390.6 | hg38 | chr11 | 134,436,735 | 134,505,173 | 68,439 |
ENST00000661684.1 | hg38 | chr11 | 134,412,305 | 134,505,665 | 93,361 |
ENST00000657630.1 | hg38 | chr11 | 134,412,284 | 134,439,007 | 26,724 |
ENST00000653028.1 | hg38 | chr11 | 134,467,611 | 134,505,661 | 38,051 |
ENST00000657630.1 | hg19 | chr11 | 134,282,178 | 134,308,901 | 26,724 |
ENST00000661684.1 | hg19 | chr11 | 134,282,199 | 134,375,559 | 93,361 |
ENST00000531319.2 | hg19 | chr11 | 134,306,367 | 134,375,553 | 69,187 |
ENST00000533390.6 | hg19 | chr11 | 134,306,629 | 134,375,067 | 68,439 |
ENST00000528482.6 | hg19 | chr11 | 134,336,079 | 134,357,809 | 21,731 |
ENST00000653028.1 | hg19 | chr11 | 134,337,505 | 134,375,555 | 38,051 |
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