MNX1-AS1 MNX1 antisense RNA 1 (head to head)
Information
- Symbol
- MNX1-AS1
- Type
- ncRNA
- Description
- MNX1 antisense RNA 1 (head to head)
- Entrez Gene ID
- 645249
- Genome
- hg19
- Position
- chr7:156,803,499-156,809,120
- Genome
- hg38
- Position
- chr7:157,010,805-157,016,426
- HGNC
- HGNC:48954 HGNC
- Ensembl
- ENSG00000243479 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
not provided | 2 | 0 |
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
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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Search word | : | |
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 | CCAT5 |
SYNONYM | MAYA |
HGNC | HGNC:48954 HGNC |
Ensembl | ENSG00000243479 Ensembl |
AllianceGenome | HGNC:48954 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000480284.1 | hg38 | chr7 | 157,010,805 | 157,016,426 | 5,622 |
ENST00000480284.1 | hg19 | chr7 | 156,803,499 | 156,809,120 | 5,622 |
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