ISG20 interferon stimulated exonuclease gene 20
Information
- Symbol
- ISG20
- Type
- protein-coding
- Description
- interferon stimulated exonuclease gene 20
- Entrez Gene ID
- 3669
- Genome
- hg19
- Position
- chr15:89,178,901-89,199,714
- Genome
- hg38
- Position
- chr15:88,635,670-88,656,483
- MIM
- 604533 OMIM
- HGNC
- HGNC:6130 HGNC
- Ensembl
- ENSG00000172183 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| Benign | 0 | 10 |
| Likely benign | 0 | 4 |
| Uncertain significance | 0 | 24 |
Ranking
| ClinVar | |
|---|---|
 |
0 |
 |
0 |
 |
0 |
 |
38 |
 |
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
[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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | Entry | Origin | Annotation | |||||||||||
Search Word
| Target data | : |
MGeND data only
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| Filtering | : |
| Name | MGeND | Type | Genome | Size | Chromosome | Start | Stop | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
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| Category | : |
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| Filtering | : |
| Name | MGeND | Type | Genome | Gene symbol | Chromosome | Genomic start | Genomic stop | Strand | Ref | Alt | ClinVar | Origin | Entry | CIViC evidence | DisGeNET entry | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | CD25 |
| SYNONYM | HEM45 |
| MIM | 604533 OMIM |
| HGNC | HGNC:6130 HGNC |
| Ensembl | ENSG00000172183 Ensembl |
| AllianceGenome | HGNC:6130 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000559876.2 | hg38 | chr15 | 88,638,953 | 88,655,531 | 16,579 |
| ENST00000379224.10 | hg38 | chr15 | 88,635,670 | 88,656,483 | 20,814 |
| ENST00000306072.10 | hg38 | chr15 | 88,639,016 | 88,656,483 | 17,468 |
| ENST00000560741.5 | hg38 | chr15 | 88,636,153 | 88,655,621 | 19,469 |
| ENST00000379224.10 | hg19 | chr15 | 89,178,901 | 89,199,714 | 20,814 |
| ENST00000560741.5 | hg19 | chr15 | 89,179,384 | 89,198,852 | 19,469 |
| ENST00000559876.2 | hg19 | chr15 | 89,182,184 | 89,198,762 | 16,579 |
| ENST00000306072.10 | hg19 | chr15 | 89,182,247 | 89,199,714 | 17,468 |
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