TLE6 TLE family member 6, subcortical maternal complex member
Information
- Symbol
- TLE6
- Type
- protein-coding
- Description
- TLE family member 6, subcortical maternal complex member
- Entrez Gene ID
- 79816
- Genome
- hg19
- Position
- chr19:2,977,562-2,995,177
- Genome
- hg38
- Position
- chr19:2,977,564-2,995,179
- MIM
- 612399 OMIM
- HGNC
- HGNC:30788 HGNC
- Ensembl
- ENSG00000104953 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Pathogenic | 0 | 8 |
Likely pathogenic | 0 | 4 |
Benign | 0 | 24 |
Likely benign | 0 | 42 |
Uncertain significance | 0 | 84 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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2 |
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154 |
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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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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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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 | GRG6 |
SYNONYM | OZEMA15 |
SYNONYM | PREMBL |
MIM | 612399 OMIM |
HGNC | HGNC:30788 HGNC |
Ensembl | ENSG00000104953 Ensembl |
AllianceGenome | HGNC:30788 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000452088.5 | hg38 | chr19 | 2,977,580 | 2,995,179 | 17,600 |
ENST00000482627.1 | hg38 | chr19 | 2,977,550 | 2,980,407 | 2,858 |
ENST00000246112.9 | hg38 | chr19 | 2,977,564 | 2,995,179 | 17,616 |
ENST00000482627.1 | hg19 | chr19 | 2,977,548 | 2,980,405 | 2,858 |
ENST00000246112.9 | hg19 | chr19 | 2,977,562 | 2,995,177 | 17,616 |
ENST00000452088.5 | hg19 | chr19 | 2,977,578 | 2,995,177 | 17,600 |
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