MIR122HG MIR122 host gene
Information
- Symbol
- MIR122HG
- Type
- ncRNA
- Description
- MIR122 host gene
- Entrez Gene ID
- 112441433
- Genome
- hg19
- Position
- chr18:56,113,475-56,120,998
- Genome
- hg38
- Position
- chr18:58,446,243-58,453,766
- HGNC
- HGNC:53821 HGNC
- Ensembl
- ENSG00000267391 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
---|
Ranking
ClinVar | |
---|---|
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
0 |
![]() |
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
|
Category | : |
|
Search word | : | |
Filtering | : |
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
|
Category | : |
|
Search word | : | |
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
|
Category | : |
|
Search word | : | |
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 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000590797.4 | hg38 | chr18 | 58,446,243 | 58,453,766 | 7,524 |
ENST00000667453.3 | hg38 | chr18 | 58,445,788 | 58,451,930 | 6,143 |
ENST00000701002.1 | hg38 | chr18 | 58,446,263 | 58,450,602 | 4,340 |
ENST00000667453.3 | hg19 | chr18 | 56,113,020 | 56,119,162 | 6,143 |
ENST00000590797.4 | hg19 | chr18 | 56,113,475 | 56,120,998 | 7,524 |
ENST00000701002.1 | hg19 | chr18 | 56,113,495 | 56,117,834 | 4,340 |
Genome browser