GXYLT1 glucoside xylosyltransferase 1
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Benign | 0 | 4 |
Likely benign | 0 | 32 |
Uncertain significance | 0 | 32 |
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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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
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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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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 |
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MGeND data only
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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 |
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SYNONYM | GLT8D3 |
MIM | 613321 OMIM |
HGNC | HGNC:27482 HGNC |
Ensembl | ENSG00000151233 Ensembl |
AllianceGenome | HGNC:27482 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000280876.6 | hg38 | chr12 | 42,087,145 | 42,144,712 | 57,568 |
ENST00000398675.8 | hg38 | chr12 | 42,081,845 | 42,144,874 | 63,030 |
ENST00000398675.8 | hg19 | chr12 | 42,475,647 | 42,538,676 | 63,030 |
ENST00000280876.6 | hg19 | chr12 | 42,480,947 | 42,538,514 | 57,568 |
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