SLX1A-SULT1A3 SLX1A-SULT1A3 readthrough (NMD candidate)
Information
- Symbol
- SLX1A-SULT1A3
- Type
- ncRNA
- Description
- SLX1A-SULT1A3 readthrough (NMD candidate)
- Entrez Gene ID
- 100526830
- Genome
- hg19
- Position
- chr16:30,205,754-30,215,627
- Genome
- hg38
- Position
- chr16:30,194,433-30,204,306
- HGNC
- HGNC:44437 HGNC
- Ensembl
- ENSG00000213599 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 3 | 0 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
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0 |
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0 |
 |
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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| Category | : |
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| Variant name | Gene | AA change | CDS | Japanese frequency |
TogoVar | MGeND | Genome | ClinVar | CIViC evidence | DisGeNET entry | COSMIC occurrence |
Prediction | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Search word | : | |
| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | HAST3 |
| SYNONYM | M-PST |
| SYNONYM | ST1A3 |
| SYNONYM | STM |
| SYNONYM | SULT1A3 |
| SYNONYM | TL-PST |
| HGNC | HGNC:44437 HGNC |
| Ensembl | ENSG00000213599 Ensembl |
| AllianceGenome | HGNC:44437 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000565342.5 | hg38 | chr16 | 30,194,433 | 30,204,306 | 9,874 |
| ENST00000565342.5 | hg19 | chr16 | 30,205,754 | 30,215,627 | 9,874 |
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