PGLS-DT PGLS divergent transcript
Information
- Symbol
- PGLS-DT
- Type
- ncRNA
- Description
- PGLS divergent transcript
- Entrez Gene ID
- 100507551
- Genome
- hg19
- Position
- chr19:17,602,196-17,622,284
- Genome
- hg38
- Position
- chr19:17,491,387-17,511,475
- HGNC
- HGNC:55274 HGNC
- Ensembl
- ENSG00000269439 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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ENST00000598141.2 | hg38 | chr19 | 17,489,800 | 17,511,492 | 21,693 |
ENST00000596643.5 | hg38 | chr19 | 17,488,990 | 17,511,889 | 22,900 |
ENST00000595116.2 | hg38 | chr19 | 17,503,436 | 17,511,514 | 8,079 |
ENST00000615939.1 | hg38 | chr19 | 17,510,100 | 17,510,850 | 751 |
ENST00000655024.1 | hg38 | chr19 | 17,491,387 | 17,511,475 | 20,089 |
ENST00000596643.5 | hg19 | chr19 | 17,599,799 | 17,622,698 | 22,900 |
ENST00000598141.2 | hg19 | chr19 | 17,600,609 | 17,622,301 | 21,693 |
ENST00000655024.1 | hg19 | chr19 | 17,602,196 | 17,622,284 | 20,089 |
ENST00000595116.2 | hg19 | chr19 | 17,614,245 | 17,622,323 | 8,079 |
ENST00000615939.1 | hg19 | chr19 | 17,620,909 | 17,621,659 | 751 |
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