MIR1200 microRNA 1200
Information
- Symbol
- MIR1200
- Type
- ncRNA
- Description
- microRNA 1200
- Entrez Gene ID
- 100302113
- Genome
- hg19
- Position
- chr7:36,958,962-36,959,037
- Genome
- hg38
- Position
- chr7:36,919,357-36,919,432
- HGNC
- HGNC:35266 HGNC
- Ensembl
- ENSG00000221325 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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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 | |||||
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Entry | Origin | Type | Annotation | Entry | Origin | Annotation |
Search Word
Target data | : |
MGeND data only
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Category | : |
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Filtering | : |
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 | MIRN1200 |
SYNONYM | hsa-mir-1200 |
HGNC | HGNC:35266 HGNC |
Ensembl | ENSG00000221325 Ensembl |
miRBase | MI0006332 |
AllianceGenome | HGNC:35266 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000408398.1 | hg38 | chr7 | 36,919,357 | 36,919,432 | 76 |
ENST00000408398.1 | hg19 | chr7 | 36,958,962 | 36,959,037 | 76 |
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