ZNF594-DT ZNF594 divergent transcript
Information
- Symbol
- ZNF594-DT
- Type
- ncRNA
- Description
- ZNF594 divergent transcript
- Entrez Gene ID
- 100130950
- Genome
- hg19
- Position
- chr17:5,095,363-5,138,900
- Genome
- hg38
- Position
- chr17:5,192,068-5,235,605
- HGNC
- HGNC:55347 HGNC
- Ensembl
- ENSG00000261879 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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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
[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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000649359.1 | hg38 | chr17 | 5,192,090 | 5,235,637 | 43,548 |
ENST00000663434.1 | hg38 | chr17 | 5,192,068 | 5,235,605 | 43,538 |
ENST00000571689.1 | hg38 | chr17 | 5,192,104 | 5,235,643 | 43,540 |
ENST00000669386.1 | hg38 | chr17 | 5,192,027 | 5,235,995 | 43,969 |
ENST00000669386.1 | hg19 | chr17 | 5,095,322 | 5,139,290 | 43,969 |
ENST00000663434.1 | hg19 | chr17 | 5,095,363 | 5,138,900 | 43,538 |
ENST00000649359.1 | hg19 | chr17 | 5,095,385 | 5,138,932 | 43,548 |
ENST00000571689.1 | hg19 | chr17 | 5,095,399 | 5,138,938 | 43,540 |
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