HS6ST1 heparan sulfate 6-O-sulfotransferase 1
Information
- Symbol
- HS6ST1
- Type
- protein-coding
- Description
- heparan sulfate 6-O-sulfotransferase 1
- Entrez Gene ID
- 9394
- Genome
- hg19
- Position
- chr2:129,023,054-129,076,442
- Genome
- hg38
- Position
- chr2:128,265,480-128,318,868
- MIM
- 604846 OMIM
- HGNC
- HGNC:5201 HGNC
- Ensembl
- ENSG00000136720 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 52 |
Likely benign | 0 | 80 |
Conflicting classifications of pathogenicity | 0 | 6 |
risk factor | 0 | 4 |
Uncertain significance | 0 | 106 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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32 |
![]() |
200 |
![]() |
4 |
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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
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MGeND data only
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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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Filtering | : |
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 | HH15 |
SYNONYM | HS6ST |
MIM | 604846 OMIM |
HGNC | HGNC:5201 HGNC |
Ensembl | ENSG00000136720 Ensembl |
AllianceGenome | HGNC:5201 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000259241.7 | hg38 | chr2 | 128,265,480 | 128,318,868 | 53,389 |
ENST00000259241.7 | hg19 | chr2 | 129,023,054 | 129,076,442 | 53,389 |
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