ST6GAL2 ST6 beta-galactoside alpha-2,6-sialyltransferase 2
Information
- Symbol
- ST6GAL2
- Type
- protein-coding
- Description
- ST6 beta-galactoside alpha-2,6-sialyltransferase 2
- Entrez Gene ID
- 84620
- Genome
- hg19
- Position
- chr2:107,418,056-107,503,563
- Genome
- hg38
- Position
- chr2:106,801,600-106,887,107
- MIM
- 608472 OMIM
- HGNC
- HGNC:10861 HGNC
- Ensembl
- ENSG00000144057 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Likely benign | 0 | 6 |
| not provided | 2 | 0 |
| Uncertain significance | 0 | 44 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
50 |
 |
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
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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| 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 | SIAT2 |
| SYNONYM | ST6GalII |
| MIM | 608472 OMIM |
| HGNC | HGNC:10861 HGNC |
| Ensembl | ENSG00000144057 Ensembl |
| AllianceGenome | HGNC:10861 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000409087.3 | hg38 | chr2 | 106,813,076 | 106,887,108 | 74,033 |
| ENST00000361686.8 | hg38 | chr2 | 106,801,600 | 106,887,107 | 85,508 |
| ENST00000409382.8 | hg38 | chr2 | 106,801,600 | 106,886,167 | 84,568 |
| ENST00000409382.8 | hg19 | chr2 | 107,418,056 | 107,502,623 | 84,568 |
| ENST00000361686.8 | hg19 | chr2 | 107,418,056 | 107,503,563 | 85,508 |
| ENST00000409087.3 | hg19 | chr2 | 107,429,532 | 107,503,564 | 74,033 |
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