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
Ranking
ClinVar
0
0
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
Category :
Search word :
Filtering :
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
Category :
Search word :
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
Category :
Search word :
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
TypeID
HGNC HGNC:27449 HGNC
Ensembl ENSG00000255545 Ensembl
AllianceGenome HGNC:27449
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
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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