B3GNT3 UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3
Information
- Symbol
- B3GNT3
- Type
- protein-coding
- Description
- UDP-GlcNAc:betaGal beta-1,3-N-acetylglucosaminyltransferase 3
- Entrez Gene ID
- 10331
- Genome
- hg19
- Position
- chr19:17,905,947-17,924,385
- Genome
- hg38
- Position
- chr19:17,795,138-17,813,576
- MIM
- 605863 OMIM
- HGNC
- HGNC:13528 HGNC
- Ensembl
- ENSG00000179913 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 8 |
Uncertain significance | 0 | 36 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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48 |
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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
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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 |
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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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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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 |
Type | ID |
---|---|
SYNONYM | B3GAL-T8 |
SYNONYM | B3GN-T3 |
SYNONYM | B3GNT-3 |
SYNONYM | HP10328 |
SYNONYM | TMEM3 |
SYNONYM | beta3Gn-T3 |
MIM | 605863 OMIM |
HGNC | HGNC:13528 HGNC |
Ensembl | ENSG00000179913 Ensembl |
AllianceGenome | HGNC:13528 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000318683.7 | hg38 | chr19 | 17,795,138 | 17,813,576 | 18,439 |
ENST00000595387.1 | hg38 | chr19 | 17,795,157 | 17,812,233 | 17,077 |
ENST00000318683.7 | hg19 | chr19 | 17,905,947 | 17,924,385 | 18,439 |
ENST00000595387.1 | hg19 | chr19 | 17,905,966 | 17,923,042 | 17,077 |
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