MEF2C-AS1 MEF2C antisense RNA 1
Information
- Symbol
- MEF2C-AS1
- Type
- ncRNA
- Description
- MEF2C antisense RNA 1
- Entrez Gene ID
- 101929423
- Genome
- hg19
- Position
- chr5:88,179,216-88,240,810
- Genome
- hg38
- Position
- chr5:88,883,399-88,944,993
- HGNC
- HGNC:48908 HGNC
- Ensembl
- ENSG00000248309 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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000514011.5 | hg38 | chr5 | 88,889,335 | 88,967,279 | 77,945 |
ENST00000691685.1 | hg38 | chr5 | 88,889,445 | 88,944,982 | 55,538 |
ENST00000508718.6 | hg38 | chr5 | 88,889,334 | 88,943,870 | 54,537 |
ENST00000700959.1 | hg38 | chr5 | 88,889,450 | 89,032,379 | 142,930 |
ENST00000513704.7 | hg38 | chr5 | 88,889,304 | 88,944,989 | 55,686 |
ENST00000702018.1 | hg38 | chr5 | 88,883,357 | 89,032,371 | 149,015 |
ENST00000685027.1 | hg38 | chr5 | 88,883,352 | 89,032,751 | 149,400 |
ENST00000514794.6 | hg38 | chr5 | 88,883,399 | 88,944,993 | 61,595 |
ENST00000684854.1 | hg38 | chr5 | 88,889,398 | 89,278,547 | 389,150 |
ENST00000514092.5 | hg38 | chr5 | 88,889,445 | 89,465,982 | 576,538 |
ENST00000701972.1 | hg38 | chr5 | 88,889,430 | 89,073,151 | 183,722 |
ENST00000513704.7 | hg19 | chr5 | 88,185,121 | 88,240,806 | 55,686 |
ENST00000514092.5 | hg19 | chr5 | 88,185,262 | 88,761,799 | 576,538 |
ENST00000684854.1 | hg19 | chr5 | 88,185,215 | 88,574,364 | 389,150 |
ENST00000685027.1 | hg19 | chr5 | 88,179,169 | 88,328,568 | 149,400 |
ENST00000702018.1 | hg19 | chr5 | 88,179,174 | 88,328,188 | 149,015 |
ENST00000514794.6 | hg19 | chr5 | 88,179,216 | 88,240,810 | 61,595 |
ENST00000514011.5 | hg19 | chr5 | 88,185,152 | 88,263,096 | 77,945 |
ENST00000691685.1 | hg19 | chr5 | 88,185,262 | 88,240,799 | 55,538 |
ENST00000700959.1 | hg19 | chr5 | 88,185,267 | 88,328,196 | 142,930 |
ENST00000508718.6 | hg19 | chr5 | 88,185,151 | 88,239,687 | 54,537 |
ENST00000701972.1 | hg19 | chr5 | 88,185,247 | 88,368,968 | 183,722 |
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