SMIM2-AS1 SMIM2 antisense RNA 1
Information
- Symbol
- SMIM2-AS1
- Type
- ncRNA
- Description
- SMIM2 antisense RNA 1
- Entrez Gene ID
- 101929212
- Genome
- hg19
- Position
- chr13:44,716,457-44,814,190
- Genome
- hg38
- Position
- chr13:44,142,321-44,240,054
- HGNC
- HGNC:42674 HGNC
- Ensembl
- ENSG00000227258 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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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 |
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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 | C13orf44-AS1 |
SYNONYM | C3orf81-AS1 |
HGNC | HGNC:42674 HGNC |
Ensembl | ENSG00000227258 Ensembl |
AllianceGenome | HGNC:42674 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000619472.1 | hg38 | chr13 | 44,143,642 | 44,154,083 | 10,442 |
ENST00000437867.6 | hg38 | chr13 | 44,142,321 | 44,240,054 | 97,734 |
ENST00000666499.1 | hg38 | chr13 | 44,142,421 | 44,240,122 | 97,702 |
ENST00000437867.6 | hg19 | chr13 | 44,716,457 | 44,814,190 | 97,734 |
ENST00000666499.1 | hg19 | chr13 | 44,716,557 | 44,814,258 | 97,702 |
ENST00000619472.1 | hg19 | chr13 | 44,717,778 | 44,728,219 | 10,442 |
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