USP27X-DT USP27X divergent transcript
Information
- Symbol
- USP27X-DT
- Type
- ncRNA
- Description
- USP27X divergent transcript
- Entrez Gene ID
- 158572
- Genome
- hg19
- Position
- chrX:49,641,327-49,643,844
- Genome
- hg38
- Position
- chrX:49,876,724-49,879,241
- HGNC
- HGNC:27249 HGNC
- Ensembl
- ENSG00000234390 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Ranking
ClinVar | |
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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
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
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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 | USP27X-AS1 |
HGNC | HGNC:27249 HGNC |
Ensembl | ENSG00000234390 Ensembl |
AllianceGenome | HGNC:27249 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000437322.2 | hg38 | chrX | 49,876,724 | 49,879,241 | 2,518 |
ENST00000437322.2 | hg19 | chrX | 49,641,327 | 49,643,844 | 2,518 |
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