MIR4428 microRNA 4428
Information
- Symbol
- MIR4428
- Type
- ncRNA
- Description
- microRNA 4428
- Entrez Gene ID
- 100616141
- Genome
- hg19
- Position
- chr1:237,634,419-237,634,491
- Genome
- hg38
- Position
- chr1:237,471,119-237,471,191
- HGNC
- HGNC:41667 HGNC
- Ensembl
- ENSG00000266262 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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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
[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 | |||||
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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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HGNC | HGNC:41667 HGNC |
Ensembl | ENSG00000266262 Ensembl |
miRBase | MI0016767 |
AllianceGenome | HGNC:41667 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000584884.1 | hg38 | chr1 | 237,471,119 | 237,471,191 | 73 |
ENST00000584884.1 | hg19 | chr1 | 237,634,419 | 237,634,491 | 73 |
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