MIR891A microRNA 891a
Information
- Symbol
- MIR891A
- Type
- ncRNA
- Description
- microRNA 891a
- Entrez Gene ID
- 100126341
- Genome
- hg19
- Position
- chrX:145,109,312-145,109,390
- Genome
- hg38
- Position
- chrX:146,027,794-146,027,872
- HGNC
- HGNC:33635 HGNC
- Ensembl
- ENSG00000216056 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 6 | 0 |
Ranking
ClinVar | |
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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
Locus Zoom
Variants
Search Word
Target data | : |
MGeND data only
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Category | : |
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Search word | : | |
Filtering | : |
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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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 | |||
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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 |
---|---|
SYNONYM | MIRN891A |
HGNC | HGNC:33635 HGNC |
Ensembl | ENSG00000216056 Ensembl |
miRBase | MI0005524 |
AllianceGenome | HGNC:33635 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000401237.1 | hg38 | chrX | 146,027,794 | 146,027,872 | 79 |
ENST00000401237.1 | hg19 | chrX | 145,109,312 | 145,109,390 | 79 |
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