TLE5 TLE family member 5, transcriptional modulator
Information
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Uncertain significance | 0 | 8 |
Ranking
ClinVar | |
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0 |
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0 |
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0 |
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8 |
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0 |
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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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 |
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Target data | : |
MGeND data only
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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 |
Type | ID |
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SYNONYM | AES |
SYNONYM | AES-1 |
SYNONYM | AES-2 |
SYNONYM | ESP1 |
SYNONYM | GRG |
SYNONYM | GRG5 |
SYNONYM | Grg-5 |
MIM | 600188 OMIM |
HGNC | HGNC:307 HGNC |
Ensembl | ENSG00000104964 Ensembl |
AllianceGenome | HGNC:307 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
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ENST00000221561.12 | hg38 | chr19 | 3,052,910 | 3,063,107 | 10,198 |
ENST00000327141.9 | hg38 | chr19 | 3,052,910 | 3,062,495 | 9,586 |
ENST00000586839.1 | hg38 | chr19 | 3,053,591 | 3,061,404 | 7,814 |
ENST00000327141.9 | hg19 | chr19 | 3,052,908 | 3,062,493 | 9,586 |
ENST00000221561.12 | hg19 | chr19 | 3,052,908 | 3,063,105 | 10,198 |
ENST00000586839.1 | hg19 | chr19 | 3,053,589 | 3,061,402 | 7,814 |
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