TLE2 TLE family member 2, transcriptional corepressor
Information
- Symbol
- TLE2
- Type
- protein-coding
- Description
- TLE family member 2, transcriptional corepressor
- Entrez Gene ID
- 7089
- Genome
- hg19
- Position
- chr19:2,997,846-3,029,011
- Genome
- hg38
- Position
- chr19:2,997,848-3,029,013
- MIM
- 601041 OMIM
- HGNC
- HGNC:11838 HGNC
- Ensembl
- ENSG00000065717 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 10 |
Uncertain significance | 0 | 88 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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94 |
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4 |
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 |
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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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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 |
---|---|
SYNONYM | ESG |
SYNONYM | ESG2 |
SYNONYM | GRG2 |
MIM | 601041 OMIM |
HGNC | HGNC:11838 HGNC |
Ensembl | ENSG00000065717 Ensembl |
AllianceGenome | HGNC:11838 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000591529.5 | hg38 | chr19 | 2,997,646 | 3,047,635 | 49,990 |
ENST00000443826.7 | hg38 | chr19 | 2,997,682 | 3,029,614 | 31,933 |
ENST00000590536.5 | hg38 | chr19 | 2,997,848 | 3,029,013 | 31,166 |
ENST00000586422.5 | hg38 | chr19 | 2,997,647 | 3,028,356 | 30,710 |
ENST00000262953.11 | hg38 | chr19 | 2,997,644 | 3,029,280 | 31,637 |
ENST00000426948.6 | hg38 | chr19 | 2,997,639 | 3,045,788 | 48,150 |
ENST00000262953.11 | hg19 | chr19 | 2,997,642 | 3,029,278 | 31,637 |
ENST00000426948.6 | hg19 | chr19 | 2,997,637 | 3,045,786 | 48,150 |
ENST00000586422.5 | hg19 | chr19 | 2,997,645 | 3,028,354 | 30,710 |
ENST00000443826.7 | hg19 | chr19 | 2,997,680 | 3,029,612 | 31,933 |
ENST00000590536.5 | hg19 | chr19 | 2,997,846 | 3,029,011 | 31,166 |
ENST00000591529.5 | hg19 | chr19 | 2,997,644 | 3,047,633 | 49,990 |
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