MIR3936HG MIR3936 host gene
Information
- Symbol
- MIR3936HG
- Type
- ncRNA
- Description
- MIR3936 host gene
- Entrez Gene ID
- 553103
- Genome
- hg19
- Position
- chr5:131,700,314-131,705,395
- Genome
- hg38
- Position
- chr5:132,364,622-132,369,703
- HGNC
- HGNC:40538 HGNC
- Ensembl
- ENSG00000233006 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar |
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Ranking
ClinVar | |
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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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SYNONYM | SLC22A5-AS1 |
HGNC | HGNC:40538 HGNC |
Ensembl | ENSG00000233006 Ensembl |
AllianceGenome | HGNC:40538 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000666504.1 | hg38 | chr5 | 132,364,622 | 132,369,703 | 5,082 |
ENST00000621103.4 | hg38 | chr5 | 132,311,285 | 132,369,916 | 58,632 |
ENST00000649993.1 | hg38 | chr5 | 132,349,815 | 132,369,659 | 19,845 |
ENST00000621103.4 | hg19 | chr5 | 131,646,978 | 131,705,608 | 58,631 |
ENST00000649993.1 | hg19 | chr5 | 131,685,508 | 131,705,351 | 19,844 |
ENST00000666504.1 | hg19 | chr5 | 131,700,314 | 131,705,395 | 5,082 |
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