MIR4520-1 microRNA 4520-1
Information
- Symbol
- MIR4520-1
- Type
- ncRNA
- Description
- microRNA 4520-1
- Entrez Gene ID
- 100616401
- Genome
- hg19
- Position
- chr17:6,558,759-6,558,828
- Genome
- hg38
- Position
- chr17:6,655,440-6,655,509
- HGNC
- HGNC:41775 HGNC
- Ensembl
- ENSG00000264468 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
 |
0 |
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0 |
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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
[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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| 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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| 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 | MIR4520A |
| SYNONYM | hsa-mir-4520-1 |
| SYNONYM | mir-4520-1 |
| HGNC | HGNC:41775 HGNC |
| Ensembl | ENSG00000264468 Ensembl |
| miRBase | MI0016886 |
| AllianceGenome | HGNC:41775 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000582609.1 | hg38 | chr17 | 6,655,440 | 6,655,509 | 70 |
| ENST00000582609.1 | hg19 | chr17 | 6,558,759 | 6,558,828 | 70 |
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