MIR4436B1 microRNA 4436b-1
Information
- Symbol
- MIR4436B1
- Type
- ncRNA
- Description
- microRNA 4436b-1
- Entrez Gene ID
- 100616123
- Genome
- hg19
- Position
- chr2:110,844,010-110,844,100
- Genome
- hg38
- Position
- chr2:110,086,433-110,086,523
- HGNC
- HGNC:41587 HGNC
- Ensembl
- ENSG00000264979 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
Ranking
| ClinVar | |
|---|---|
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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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| 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
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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 | MIR4436B |
| SYNONYM | hsa-mir-4436b-1 |
| HGNC | HGNC:41587 HGNC |
| Ensembl | ENSG00000264979 Ensembl |
| miRBase | MI0017425 |
| AllianceGenome | HGNC:41587 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000583272.1 | hg38 | chr2 | 110,086,433 | 110,086,523 | 91 |
| ENST00000583272.1 | hg19 | chr2 | 110,844,010 | 110,844,100 | 91 |
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