MIR381HG MIR381 host gene
Information
- Symbol
- MIR381HG
- Type
- ncRNA
- Description
- MIR381 host gene
- Entrez Gene ID
- 378881
- Genome
- hg19
- Position
- chr14:101,509,245-101,522,581
- Genome
- hg38
- Position
- chr14:101,042,908-101,056,244
- HGNC
- HGNC:20136 HGNC
- Ensembl
- ENSG00000223403 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
| MGeND | ClinVar |
|---|
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 | |||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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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| 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 | C14orf89 |
| SYNONYM | NCRNA00225 |
| HGNC | HGNC:20136 HGNC |
| Ensembl | ENSG00000223403 Ensembl |
| AllianceGenome | HGNC:20136 |
| Descrption | Source | Links |
|---|
| ID | Genome | Chromosome | Start | End | Length |
|---|---|---|---|---|---|
| ENST00000553692.1 | hg38 | chr14 | 101,045,157 | 101,051,795 | 6,639 |
| ENST00000665682.1 | hg38 | chr14 | 101,069,931 | 101,072,028 | 2,098 |
| ENST00000665822.1 | hg38 | chr14 | 101,068,283 | 101,072,931 | 4,649 |
| ENST00000699460.1 | hg38 | chr14 | 101,042,908 | 101,056,244 | 13,337 |
| ENST00000699461.1 | hg38 | chr14 | 101,055,035 | 101,072,934 | 17,900 |
| ENST00000452349.2 | hg38 | chr14 | 101,069,192 | 101,072,937 | 3,746 |
| ENST00000429368.2 | hg38 | chr14 | 101,069,911 | 101,072,937 | 3,027 |
| ENST00000699460.1 | hg19 | chr14 | 101,509,245 | 101,522,581 | 13,337 |
| ENST00000553692.1 | hg19 | chr14 | 101,511,494 | 101,518,132 | 6,639 |
| ENST00000699461.1 | hg19 | chr14 | 101,521,372 | 101,539,271 | 17,900 |
| ENST00000665822.1 | hg19 | chr14 | 101,534,620 | 101,539,268 | 4,649 |
| ENST00000452349.2 | hg19 | chr14 | 101,535,529 | 101,539,274 | 3,746 |
| ENST00000429368.2 | hg19 | chr14 | 101,536,248 | 101,539,274 | 3,027 |
| ENST00000665682.1 | hg19 | chr14 | 101,536,268 | 101,538,365 | 2,098 |
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