ST6GALNAC2 ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2
Information
- Symbol
- ST6GALNAC2
- Type
- protein-coding
- Description
- ST6 N-acetylgalactosaminide alpha-2,6-sialyltransferase 2
- Entrez Gene ID
- 10610
- Genome
- hg19
- Position
- chr17:74,561,459-74,581,942
- Genome
- hg38
- Position
- chr17:76,565,377-76,585,860
- MIM
- 610137 OMIM
- HGNC
- HGNC:10867 HGNC
- Ensembl
- ENSG00000070731 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Uncertain significance | 0 | 64 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
64 |
 |
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 | SAITL1 |
| SYNONYM | SIAT7 |
| SYNONYM | SIAT7B |
| SYNONYM | SIATL1 |
| SYNONYM | ST6GalNAII |
| SYNONYM | STHM |
| MIM | 610137 OMIM |
| HGNC | HGNC:10867 HGNC |
| Ensembl | ENSG00000070731 Ensembl |
| AllianceGenome | HGNC:10867 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000225276.10 | hg38 | chr17 | 76,565,377 | 76,585,860 | 20,484 |
| ENST00000225276.10 | hg19 | chr17 | 74,561,459 | 74,581,942 | 20,484 |
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