MIR153-2 microRNA 153-2
Information
- Symbol
- MIR153-2
- Type
- ncRNA
- Description
- microRNA 153-2
- Entrez Gene ID
- 406945
- Genome
- hg19
- Position
- chr7:157,367,028-157,367,114
- Genome
- hg38
- Position
- chr7:157,574,336-157,574,422
- HGNC
- HGNC:31540 HGNC
- Ensembl
- ENSG00000207960 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 2 | 0 |
Ranking
ClinVar | |
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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
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 |
Type | ID |
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SYNONYM | MIRN153-2 |
SYNONYM | mir-153-2 |
HGNC | HGNC:31540 HGNC |
Ensembl | ENSG00000207960 Ensembl |
miRBase | MI0000464 |
AllianceGenome | HGNC:31540 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000385225.1 | hg38 | chr7 | 157,574,336 | 157,574,422 | 87 |
ENST00000385225.1 | hg19 | chr7 | 157,367,028 | 157,367,114 | 87 |
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