UGGT2 UDP-glucose glycoprotein glucosyltransferase 2
Information
- Symbol
- UGGT2
- Type
- protein-coding
- Description
- UDP-glucose glycoprotein glucosyltransferase 2
- Entrez Gene ID
- 55757
- Genome
- hg19
- Position
- chr13:96,453,834-96,705,655
- Genome
- hg38
- Position
- chr13:95,801,580-96,053,401
- MIM
- 605898 OMIM
- HGNC
- HGNC:15664 HGNC
- Ensembl
- ENSG00000102595 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 10 |
| Likely benign | 0 | 22 |
| Uncertain significance | 0 | 166 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
2 |
 |
194 |
 |
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
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| Category | : |
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| 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 | HUGT2 |
| SYNONYM | UGCGL2 |
| SYNONYM | UGT2 |
| MIM | 605898 OMIM |
| HGNC | HGNC:15664 HGNC |
| Ensembl | ENSG00000102595 Ensembl |
| AllianceGenome | HGNC:15664 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000376747.8 | hg38 | chr13 | 95,801,580 | 96,053,401 | 251,822 |
| ENST00000397618.7 | hg38 | chr13 | 95,984,910 | 96,053,400 | 68,491 |
| ENST00000376714.7 | hg38 | chr13 | 95,983,524 | 96,053,482 | 69,959 |
| ENST00000376712.4 | hg38 | chr13 | 95,990,145 | 96,053,393 | 63,249 |
| ENST00000376747.8 | hg19 | chr13 | 96,453,834 | 96,705,655 | 251,822 |
| ENST00000376714.7 | hg19 | chr13 | 96,635,778 | 96,705,736 | 69,959 |
| ENST00000397618.7 | hg19 | chr13 | 96,637,164 | 96,705,654 | 68,491 |
| ENST00000376712.4 | hg19 | chr13 | 96,642,399 | 96,705,647 | 63,249 |
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