HS3ST6 heparan sulfate-glucosamine 3-sulfotransferase 6
Information
- Symbol
- HS3ST6
- Type
- protein-coding
- Description
- heparan sulfate-glucosamine 3-sulfotransferase 6
- Entrez Gene ID
- 64711
- Genome
- hg19
- Position
- chr16:1,961,476-1,968,416
- Genome
- hg38
- Position
- chr16:1,911,475-1,918,415
- MIM
- 619210 OMIM
- HGNC
- HGNC:14178 HGNC
- Ensembl
- ENSG00000162040 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 2 |
Likely benign | 0 | 4 |
Uncertain significance | 0 | 66 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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68 |
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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 | 3-OST-6 |
SYNONYM | 3OST6 |
SYNONYM | HAE8 |
SYNONYM | HS3ST5 |
MIM | 619210 OMIM |
HGNC | HGNC:14178 HGNC |
Ensembl | ENSG00000162040 Ensembl |
AllianceGenome | HGNC:14178 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000454677.3 | hg38 | chr16 | 1,911,475 | 1,918,415 | 6,941 |
ENST00000454677.3 | hg19 | chr16 | 1,961,476 | 1,968,416 | 6,941 |
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