MGAT5B alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B
Information
- Symbol
- MGAT5B
- Type
- protein-coding
- Description
- alpha-1,6-mannosylglycoprotein 6-beta-N-acetylglucosaminyltransferase B
- Entrez Gene ID
- 146664
- Genome
- hg19
- Position
- chr17:74,868,729-74,946,464
- Genome
- hg38
- Position
- chr17:76,872,647-76,950,382
- MIM
- 612441 OMIM
- HGNC
- HGNC:24140 HGNC
- Ensembl
- ENSG00000167889 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 10 |
| Uncertain significance | 0 | 82 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
92 |
 |
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
|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | GnT-IX |
| SYNONYM | GnT-VB |
| MIM | 612441 OMIM |
| HGNC | HGNC:24140 HGNC |
| Ensembl | ENSG00000167889 Ensembl |
| AllianceGenome | HGNC:24140 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000569840.7 | hg38 | chr17 | 76,868,404 | 76,950,393 | 81,990 |
| ENST00000301618.8 | hg38 | chr17 | 76,868,456 | 76,950,377 | 81,922 |
| ENST00000428789.6 | hg38 | chr17 | 76,872,647 | 76,950,382 | 77,736 |
| ENST00000565675.1 | hg38 | chr17 | 76,868,716 | 76,882,527 | 13,812 |
| ENST00000569840.7 | hg19 | chr17 | 74,864,486 | 74,946,475 | 81,990 |
| ENST00000301618.8 | hg19 | chr17 | 74,864,538 | 74,946,459 | 81,922 |
| ENST00000565675.1 | hg19 | chr17 | 74,864,798 | 74,878,609 | 13,812 |
| ENST00000428789.6 | hg19 | chr17 | 74,868,729 | 74,946,464 | 77,736 |
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