B3GNT8 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8

Information
Symbol
B3GNT8
Type
protein-coding
Description
UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 8
Entrez Gene ID
374907
Genome
hg19
Position
chr19:41,931,264-41,934,635
Genome
hg38
Position
chr19:41,425,359-41,428,730
MIM
615357 OMIM
HGNC
HGNC:24139 HGNC
Ensembl
ENSG00000177191 Ensembl
Links
NCBI Gene Cards OncoKB
Clinical Significance
MGeND ClinVar
Benign 0 24
Likely benign 0 4
Uncertain significance 0 76
Ranking
ClinVar
0
0
0
104
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 :
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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
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
SYNONYM B3GALT7
SYNONYM BGALT15
SYNONYM beta3Gn-T8
MIM 615357 OMIM
HGNC HGNC:24139 HGNC
Ensembl ENSG00000177191 Ensembl
AllianceGenome HGNC:24139
DescrptionSourceLinks
IDGenomeChromosomeStartEndLength
ENST00000691102.1 hg38 chr19 41,425,359 41,427,374 2,016
ENST00000321702.2 hg38 chr19 41,425,359 41,428,730 3,372
ENST00000691102.1 hg19 chr19 41,931,264 41,933,279 2,016
ENST00000321702.2 hg19 chr19 41,931,264 41,934,635 3,372
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