MGST3 microsomal glutathione S-transferase 3
Information
- Symbol
- MGST3
- Type
- protein-coding
- Description
- microsomal glutathione S-transferase 3
- Entrez Gene ID
- 4259
- Genome
- hg19
- Position
- chr1:165,600,471-165,625,373
- Genome
- hg38
- Position
- chr1:165,631,234-165,656,136
- MIM
- 604564 OMIM
- HGNC
- HGNC:7064 HGNC
- Ensembl
- ENSG00000143198 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
association | 0 | 10 |
protective | 0 | 2 |
Uncertain significance | 0 | 14 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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16 |
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12 |
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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Target data | : |
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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Search word | : | |
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 | GST-3 |
SYNONYM | GST-III |
MIM | 604564 OMIM |
HGNC | HGNC:7064 HGNC |
Ensembl | ENSG00000143198 Ensembl |
AllianceGenome | HGNC:7064 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000627653.1 | hg38 | chr1 | 165,632,240 | 165,656,133 | 23,894 |
ENST00000367883.3 | hg38 | chr1 | 165,632,063 | 165,655,620 | 23,558 |
ENST00000367888.8 | hg38 | chr1 | 165,631,213 | 165,661,796 | 30,584 |
ENST00000367889.8 | hg38 | chr1 | 165,631,234 | 165,656,136 | 24,903 |
ENST00000367884.6 | hg38 | chr1 | 165,631,255 | 165,655,620 | 24,366 |
ENST00000367885.5 | hg38 | chr1 | 165,631,240 | 165,655,620 | 24,381 |
ENST00000367888.8 | hg19 | chr1 | 165,600,450 | 165,631,033 | 30,584 |
ENST00000367889.8 | hg19 | chr1 | 165,600,471 | 165,625,373 | 24,903 |
ENST00000367885.5 | hg19 | chr1 | 165,600,477 | 165,624,857 | 24,381 |
ENST00000367884.6 | hg19 | chr1 | 165,600,492 | 165,624,857 | 24,366 |
ENST00000367883.3 | hg19 | chr1 | 165,601,300 | 165,624,857 | 23,558 |
ENST00000627653.1 | hg19 | chr1 | 165,601,477 | 165,625,370 | 23,894 |
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