LINC00032 long intergenic non-protein coding RNA 32
Information
- Symbol
- LINC00032
- Type
- ncRNA
- Description
- long intergenic non-protein coding RNA 32
- Entrez Gene ID
- 158035
- Genome
- hg19
- Position
- chr9:27,245,682-27,282,791
- Genome
- hg38
- Position
- chr9:27,245,684-27,282,793
- HGNC
- HGNC:16506 HGNC
- Ensembl
- ENSG00000291187 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 |
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 | C9orf14 |
SYNONYM | NCRNA00032 |
HGNC | HGNC:16506 HGNC |
Ensembl | ENSG00000291187 Ensembl |
AllianceGenome | HGNC:16506 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000640247.1 | hg38 | chr9 | 27,278,307 | 27,284,869 | 6,563 |
ENST00000640190.1 | hg38 | chr9 | 27,245,684 | 27,282,793 | 37,110 |
ENST00000640190.1 | hg19 | chr9 | 27,245,682 | 27,282,791 | 37,110 |
ENST00000640247.1 | hg19 | chr9 | 27,278,305 | 27,284,867 | 6,563 |
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