TCEAL4 transcription elongation factor A like 4
Information
- Symbol
- TCEAL4
- Type
- protein-coding
- Description
- transcription elongation factor A like 4
- Entrez Gene ID
- 79921
- Genome
- hg19
- Position
- chrX:102,831,159-102,842,446
- Genome
- hg38
- Position
- chrX:103,576,231-103,587,518
- HGNC
- HGNC:26121 HGNC
- Ensembl
- ENSG00000133142 Ensembl
- Links
- NCBI Gene Cards OncoKB
Clinical Significance
MGeND | ClinVar | |
---|---|---|
Likely benign | 0 | 8 |
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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18 |
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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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Category | : |
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Filtering | : |
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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Category | : |
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Search word | : | |
Filtering | : |
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 | |||
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
Entry | Origin | Type | Annotation |
Type | ID |
---|---|
SYNONYM | NPD017 |
SYNONYM | WEX7 |
HGNC | HGNC:26121 HGNC |
Ensembl | ENSG00000133142 Ensembl |
AllianceGenome | HGNC:26121 |
Descrption | Source | Links |
---|
ID | Genome | Chromosome | Start | End | Length |
---|---|---|---|---|---|
ENST00000415568.2 | hg38 | chrX | 103,585,515 | 103,587,502 | 1,988 |
ENST00000494801.5 | hg38 | chrX | 103,585,563 | 103,587,526 | 1,964 |
ENST00000472745.1 | hg38 | chrX | 103,585,533 | 103,587,694 | 2,162 |
ENST00000372629.4 | hg38 | chrX | 103,576,231 | 103,587,518 | 11,288 |
ENST00000472484.6 | hg38 | chrX | 103,585,515 | 103,587,729 | 2,215 |
ENST00000468024.5 | hg38 | chrX | 103,585,492 | 103,587,518 | 2,027 |
ENST00000372629.4 | hg19 | chrX | 102,831,159 | 102,842,446 | 11,288 |
ENST00000468024.5 | hg19 | chrX | 102,840,420 | 102,842,446 | 2,027 |
ENST00000415568.2 | hg19 | chrX | 102,840,443 | 102,842,430 | 1,988 |
ENST00000472484.6 | hg19 | chrX | 102,840,443 | 102,842,657 | 2,215 |
ENST00000472745.1 | hg19 | chrX | 102,840,461 | 102,842,622 | 2,162 |
ENST00000494801.5 | hg19 | chrX | 102,840,491 | 102,842,454 | 1,964 |
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