TCEAL8 transcription elongation factor A like 8
Information
- Symbol
- TCEAL8
- Type
- protein-coding
- Description
- transcription elongation factor A like 8
- Entrez Gene ID
- 90843
- Genome
- hg19
- Position
- chrX:102,507,923-102,510,083
- Genome
- hg38
- Position
- chrX:103,252,995-103,255,155
- HGNC
- HGNC:28683 HGNC
- Ensembl
- ENSG00000180964 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 2 |
not provided | 6 | 0 |
Uncertain significance | 0 | 10 |
Ranking
ClinVar | |
---|---|
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0 |
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0 |
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0 |
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12 |
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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
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
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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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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 |
Descrption | Source | Links |
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ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000360000.8 | hg38 | chrX | 103,252,995 | 103,255,185 | 2,191 |
ENST00000372685.8 | hg38 | chrX | 103,252,995 | 103,255,155 | 2,161 |
ENST00000372685.8 | hg19 | chrX | 102,507,923 | 102,510,083 | 2,161 |
ENST00000360000.8 | hg19 | chrX | 102,507,923 | 102,510,113 | 2,191 |
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