TPST2 tyrosylprotein sulfotransferase 2
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 2 | 36 |
Ranking
ClinVar | |
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0 |
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36 |
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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
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 |
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Target data | : |
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 | TANGO13B |
SYNONYM | TPST-2 |
MIM | 603126 OMIM |
HGNC | HGNC:12021 HGNC |
Ensembl | ENSG00000128294 Ensembl |
AllianceGenome | HGNC:12021 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000398110.6 | hg38 | chr22 | 26,525,746 | 26,565,368 | 39,623 |
ENST00000454778.6 | hg38 | chr22 | 26,524,082 | 26,550,653 | 26,572 |
ENST00000338754.9 | hg38 | chr22 | 26,521,996 | 26,590,132 | 68,137 |
ENST00000403880.5 | hg38 | chr22 | 26,525,746 | 26,596,717 | 70,972 |
ENST00000338754.9 | hg19 | chr22 | 26,917,962 | 26,986,096 | 68,135 |
ENST00000454778.6 | hg19 | chr22 | 26,920,048 | 26,946,619 | 26,572 |
ENST00000398110.6 | hg19 | chr22 | 26,921,712 | 26,961,334 | 39,623 |
ENST00000403880.5 | hg19 | chr22 | 26,921,712 | 26,992,681 | 70,970 |
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