TEX26-AS1 TEX26 antisense RNA 1
Information
- Symbol
- TEX26-AS1
- Type
- ncRNA
- Description
- TEX26 antisense RNA 1
- Entrez Gene ID
- 100507064
- Genome
- hg19
- Position
- chr13:31,456,978-31,506,745
- Genome
- hg38
- Position
- chr13:30,882,841-30,932,608
- HGNC
- HGNC:42784 HGNC
- Ensembl
- ENSG00000224743 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 | LINC00447 |
HGNC | HGNC:42784 HGNC |
Ensembl | ENSG00000224743 Ensembl |
AllianceGenome | HGNC:42784 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000592950.5 | hg38 | chr13 | 30,881,933 | 30,931,283 | 49,351 |
ENST00000585870.6 | hg38 | chr13 | 30,882,841 | 30,932,608 | 49,768 |
ENST00000586464.5 | hg38 | chr13 | 30,916,184 | 30,931,429 | 15,246 |
ENST00000591300.2 | hg38 | chr13 | 30,922,630 | 30,933,431 | 10,802 |
ENST00000411835.6 | hg38 | chr13 | 30,930,672 | 30,932,584 | 1,913 |
ENST00000664586.1 | hg38 | chr13 | 30,882,860 | 30,932,598 | 49,739 |
ENST00000589840.1 | hg38 | chr13 | 30,930,846 | 30,932,253 | 1,408 |
ENST00000585582.1 | hg38 | chr13 | 30,928,658 | 30,931,542 | 2,885 |
ENST00000585870.6 | hg19 | chr13 | 31,456,978 | 31,506,745 | 49,768 |
ENST00000586464.5 | hg19 | chr13 | 31,490,321 | 31,505,566 | 15,246 |
ENST00000411835.6 | hg19 | chr13 | 31,504,809 | 31,506,721 | 1,913 |
ENST00000585582.1 | hg19 | chr13 | 31,502,795 | 31,505,679 | 2,885 |
ENST00000592950.5 | hg19 | chr13 | 31,456,070 | 31,505,420 | 49,351 |
ENST00000591300.2 | hg19 | chr13 | 31,496,767 | 31,507,568 | 10,802 |
ENST00000664586.1 | hg19 | chr13 | 31,456,997 | 31,506,735 | 49,739 |
ENST00000589840.1 | hg19 | chr13 | 31,504,983 | 31,506,390 | 1,408 |
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