CSE1L-DT CSE1L divergent transcript
Information
- Symbol
- CSE1L-DT
- Type
- ncRNA
- Description
- CSE1L divergent transcript
- Entrez Gene ID
- 102723483
- Genome
- hg19
- Position
- chr20:47,657,001-47,662,705
- Genome
- hg38
- Position
- chr20:49,040,464-49,046,168
- HGNC
- HGNC:51232 HGNC
- Ensembl
- ENSG00000227431 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 1 | 0 |
Ranking
ClinVar | |
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0 |
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0 |
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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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Category | : |
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Search word | : | |
Filtering | : |
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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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 | |||
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Entry | Origin | Type | Annotation |
Search Word
Target data | : |
MGeND data only
|
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 | CSE1L-AS1 |
HGNC | HGNC:51232 HGNC |
Ensembl | ENSG00000227431 Ensembl |
AllianceGenome | HGNC:51232 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000656931.1 | hg38 | chr20 | 49,040,464 | 49,046,168 | 5,705 |
ENST00000656931.1 | hg19 | chr20 | 47,657,001 | 47,662,705 | 5,705 |
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