SOX1-OT SOX1 overlapping transcript
Information
- Symbol
- SOX1-OT
- Type
- ncRNA
- Description
- SOX1 overlapping transcript
- Entrez Gene ID
- 100505996
- Genome
- hg19
- Position
- chr13:112,711,159-112,754,682
- Genome
- hg38
- Position
- chr13:112,056,845-112,100,368
- HGNC
- HGNC:42733 HGNC
- Ensembl
- ENSG00000224243 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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0 |
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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 |
Search Word
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 |
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SYNONYM | LINC00403 |
HGNC | HGNC:42733 HGNC |
Ensembl | ENSG00000224243 Ensembl |
AllianceGenome | HGNC:42733 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000657728.1 | hg38 | chr13 | 112,088,047 | 112,108,014 | 19,968 |
ENST00000663025.1 | hg38 | chr13 | 112,056,845 | 112,100,368 | 43,524 |
ENST00000663025.1 | hg19 | chr13 | 112,711,159 | 112,754,682 | 43,524 |
ENST00000657728.1 | hg19 | chr13 | 112,742,361 | 112,762,328 | 19,968 |
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