MIR3690 microRNA 3690
Information
- Symbol
- MIR3690
- Type
- ncRNA
- Description
- microRNA 3690
- Entrez Gene ID
- 100500894
- Genome
- hg19
- Position
- chrY:1,362,811-1,362,885
- Genome
- hg38
- Position
- chrX:1,293,918-1,293,992
- Genome
- hg38
- Position
- chrY:1,293,918-1,293,992
- HGNC
- HGNC:38967 HGNC
- Ensembl
- ENSG00000265658 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar | |
|---|---|---|
| not provided | 7 | 0 |
Ranking
| ClinVar | |
|---|---|
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0 |
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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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| 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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| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | ||||||||||||||
Search Word
| Target data | : |
MGeND data only
|
| 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 | |||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Entry | Origin | Type | Annotation | |||||||||||||||
| Type | ID |
|---|---|
| SYNONYM | MIR3690-1 |
| SYNONYM | MIR3690-2 |
| SYNONYM | hsa-mir-3690-1 |
| SYNONYM | hsa-mir-3690-2 |
| SYNONYM | mir-3690-1 |
| SYNONYM | mir-3690-2 |
| HGNC | HGNC:38967 HGNC |
| Ensembl | ENSG00000265658 Ensembl |
| Ensembl | ENSG00000292355 Ensembl |
| miRBase | MI0016091 |
| AllianceGenome | HGNC:38967 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000580266.6 | hg38 | chrX | 1,293,918 | 1,293,992 | 75 |
| ENST00000711140.1 | hg38 | chrY | 1,293,918 | 1,293,992 | 75 |
| ENST00000580266.1 | hg19 | chrY | 1,362,811 | 1,362,885 | 75 |
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